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Triamcinolone acetonide-d6

Cat No.:V48154 Purity: ≥98%
Triamcinolone acetonide-d6 is the deuterium labelled form of Triamcinolone acetonide.
Triamcinolone acetonide-d6
Triamcinolone acetonide-d6 Chemical Structure CAS No.: 352431-33-5
Product category: New3
This product is for research use only, not for human use. We do not sell to patients.
Size Price
500mg
1g
Other Sizes

Other Forms of Triamcinolone acetonide-d6:

  • 21-Carboxylic acid triamcinolone acetonide
  • Triamcinolone acetonide acetate
  • 6b-Hydroxy triamcinolone acetonide
  • Triamcinolone acetonide-d7-1
  • Triamcinolone Acetonide
Official Supplier of:
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Top Publications Citing lnvivochem Products
Product Description
Triamcinolone acetonide-d6 is the deuterium labelled form of Triamcinolone acetonide. Triamcinolone acetonide is eight times more effective than prednisone.
Biological Activity I Assay Protocols (From Reference)
ln Vitro
Stable heavy isotopes of hydrogen, carbon and other elements have been incorporated into drug molecules, primarily as quantitative tracers during drug development. Deuteration is of concern because of its possible impact on the pharmacokinetics and metabolic characteristics of drugs [1].
References

[1]. http://en.wikipedia.org/wiki/Triamcinolone_acetonide.

[2]. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019;53(2):211-216.

[3]. Glucocorticoids improve severe or critical COVID-19 by activating ACE2 and reducing IL-6 levels. Int J Biol Sci 2020; 16(13):2382-2391.

Additional Infomation
Triamcinolone acetonide esters. It is an anti-inflammatory glucocorticoid used topically to treat various skin conditions. In some cases, it can also be administered via intralesional, intramuscular, or intra-articular injection.
These protocols are for reference only. InvivoChem does not independently validate these methods.
Physicochemical Properties
Molecular Formula
C24H31FO6
Molecular Weight
440.53472161293
Exact Mass
440.248
CAS #
352431-33-5
Related CAS #
Triamcinolone acetonide;76-25-5
PubChem CID
633097
Appearance
White to off-white solid powder
Density
1.3±0.1 g/cm3
Boiling Point
576.9±50.0 °C at 760 mmHg
Flash Point
302.7±30.1 °C
Vapour Pressure
0.0±3.6 mmHg at 25°C
Index of Refraction
1.589
LogP
2.5
Hydrogen Bond Donor Count
2
Hydrogen Bond Acceptor Count
7
Rotatable Bond Count
2
Heavy Atom Count
31
Complexity
925
Defined Atom Stereocenter Count
0
SMILES
F[C@@]12[C@]3(C=CC(C=C3CCC1C1C[C@@H]3[C@](C(CO)=O)([C@@]1(C)C[C@@H]2O)OC(C([2H])([2H])[2H])(C([2H])([2H])[2H])O3)=O)C
InChi Key
YNDXUCZADRHECN-UHFFFAOYSA-N
InChi Code
InChI=1S/C24H31FO6/c1-20(2)30-19-10-16-15-6-5-13-9-14(27)7-8-21(13,3)23(15,25)17(28)11-22(16,4)24(19,31-20)18(29)12-26/h7-9,15-17,19,26,28H,5-6,10-12H2,1-4H3
Chemical Name
12-fluoro-11-hydroxy-8-(2-hydroxyacetyl)-6,6,9,13-tetramethyl-5,7-dioxapentacyclo[10.8.0.02,9.04,8.013,18]icosa-14,17-dien-16-one
HS Tariff Code
2934.99.9001
Storage

Powder      -20°C    3 years

                     4°C     2 years

In solvent   -80°C    6 months

                  -20°C    1 month

Shipping Condition
Room temperature (This product is stable at ambient temperature for a few days during ordinary shipping and time spent in Customs)
Solubility Data
Solubility (In Vitro)
May dissolve in DMSO (in most cases), if not, try other solvents such as H2O, Ethanol, or DMF with a minute amount of products to avoid loss of samples
Solubility (In Vivo)
Note: Listed below are some common formulations that may be used to formulate products with low water solubility (e.g. < 1 mg/mL), you may test these formulations using a minute amount of products to avoid loss of samples.

Injection Formulations
(e.g. IP/IV/IM/SC)
Injection Formulation 1: DMSO : Tween 80: Saline = 10 : 5 : 85 (i.e. 100 μL DMSO stock solution 50 μL Tween 80 850 μL Saline)
*Preparation of saline: Dissolve 0.9 g of sodium chloride in 100 mL ddH ₂ O to obtain a clear solution.
Injection Formulation 2: DMSO : PEG300Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL DMSO 400 μLPEG300 50 μL Tween 80 450 μL Saline)
Injection Formulation 3: DMSO : Corn oil = 10 : 90 (i.e. 100 μL DMSO 900 μL Corn oil)
Example: Take the Injection Formulation 3 (DMSO : Corn oil = 10 : 90) as an example, if 1 mL of 2.5 mg/mL working solution is to be prepared, you can take 100 μL 25 mg/mL DMSO stock solution and add to 900 μL corn oil, mix well to obtain a clear or suspension solution (2.5 mg/mL, ready for use in animals).
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Injection Formulation 4: DMSO : 20% SBE-β-CD in saline = 10 : 90 [i.e. 100 μL DMSO 900 μL (20% SBE-β-CD in saline)]
*Preparation of 20% SBE-β-CD in Saline (4°C,1 week): Dissolve 2 g SBE-β-CD in 10 mL saline to obtain a clear solution.
Injection Formulation 5: 2-Hydroxypropyl-β-cyclodextrin : Saline = 50 : 50 (i.e. 500 μL 2-Hydroxypropyl-β-cyclodextrin 500 μL Saline)
Injection Formulation 6: DMSO : PEG300 : castor oil : Saline = 5 : 10 : 20 : 65 (i.e. 50 μL DMSO 100 μLPEG300 200 μL castor oil 650 μL Saline)
Injection Formulation 7: Ethanol : Cremophor : Saline = 10: 10 : 80 (i.e. 100 μL Ethanol 100 μL Cremophor 800 μL Saline)
Injection Formulation 8: Dissolve in Cremophor/Ethanol (50 : 50), then diluted by Saline
Injection Formulation 9: EtOH : Corn oil = 10 : 90 (i.e. 100 μL EtOH 900 μL Corn oil)
Injection Formulation 10: EtOH : PEG300Tween 80 : Saline = 10 : 40 : 5 : 45 (i.e. 100 μL EtOH 400 μLPEG300 50 μL Tween 80 450 μL Saline)


Oral Formulations
Oral Formulation 1: Suspend in 0.5% CMC Na (carboxymethylcellulose sodium)
Oral Formulation 2: Suspend in 0.5% Carboxymethyl cellulose
Example: Take the Oral Formulation 1 (Suspend in 0.5% CMC Na) as an example, if 100 mL of 2.5 mg/mL working solution is to be prepared, you can first prepare 0.5% CMC Na solution by measuring 0.5 g CMC Na and dissolve it in 100 mL ddH2O to obtain a clear solution; then add 250 mg of the product to 100 mL 0.5% CMC Na solution, to make the suspension solution (2.5 mg/mL, ready for use in animals).
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Oral Formulation 3: Dissolved in PEG400
Oral Formulation 4: Suspend in 0.2% Carboxymethyl cellulose
Oral Formulation 5: Dissolve in 0.25% Tween 80 and 0.5% Carboxymethyl cellulose
Oral Formulation 6: Mixing with food powders


Note: Please be aware that the above formulations are for reference only. InvivoChem strongly recommends customers to read literature methods/protocols carefully before determining which formulation you should use for in vivo studies, as different compounds have different solubility properties and have to be formulated differently.

 (Please use freshly prepared in vivo formulations for optimal results.)
Preparing Stock Solutions 1 mg 5 mg 10 mg
1 mM 2.2700 mL 11.3500 mL 22.6999 mL
5 mM 0.4540 mL 2.2700 mL 4.5400 mL
10 mM 0.2270 mL 1.1350 mL 2.2700 mL

*Note: Please select an appropriate solvent for the preparation of stock solution based on your experiment needs. For most products, DMSO can be used for preparing stock solutions (e.g. 5 mM, 10 mM, or 20 mM concentration); some products with high aqueous solubility may be dissolved in water directly. Solubility information is available at the above Solubility Data section. Once the stock solution is prepared, aliquot it to routine usage volumes and store at -20°C or -80°C. Avoid repeated freeze and thaw cycles.

Calculator

Molarity Calculator allows you to calculate the mass, volume, and/or concentration required for a solution, as detailed below:

  • Calculate the Mass of a compound required to prepare a solution of known volume and concentration
  • Calculate the Volume of solution required to dissolve a compound of known mass to a desired concentration
  • Calculate the Concentration of a solution resulting from a known mass of compound in a specific volume
An example of molarity calculation using the molarity calculator is shown below:
What is the mass of compound required to make a 10 mM stock solution in 5 ml of DMSO given that the molecular weight of the compound is 350.26 g/mol?
  • Enter 350.26 in the Molecular Weight (MW) box
  • Enter 10 in the Concentration box and choose the correct unit (mM)
  • Enter 5 in the Volume box and choose the correct unit (mL)
  • Click the “Calculate” button
  • The answer of 17.513 mg appears in the Mass box. In a similar way, you may calculate the volume and concentration.

Dilution Calculator allows you to calculate how to dilute a stock solution of known concentrations. For example, you may Enter C1, C2 & V2 to calculate V1, as detailed below:

What volume of a given 10 mM stock solution is required to make 25 ml of a 25 μM solution?
Using the equation C1V1 = C2V2, where C1=10 mM, C2=25 μM, V2=25 ml and V1 is the unknown:
  • Enter 10 into the Concentration (Start) box and choose the correct unit (mM)
  • Enter 25 into the Concentration (End) box and select the correct unit (mM)
  • Enter 25 into the Volume (End) box and choose the correct unit (mL)
  • Click the “Calculate” button
  • The answer of 62.5 μL (0.1 ml) appears in the Volume (Start) box
g/mol

Molecular Weight Calculator allows you to calculate the molar mass and elemental composition of a compound, as detailed below:

Note: Chemical formula is case sensitive: C12H18N3O4  c12h18n3o4
Instructions to calculate molar mass (molecular weight) of a chemical compound:
  • To calculate molar mass of a chemical compound, please enter the chemical/molecular formula and click the “Calculate’ button.
Definitions of molecular mass, molecular weight, molar mass and molar weight:
  • Molecular mass (or molecular weight) is the mass of one molecule of a substance and is expressed in the unified atomic mass units (u). (1 u is equal to 1/12 the mass of one atom of carbon-12)
  • Molar mass (molar weight) is the mass of one mole of a substance and is expressed in g/mol.
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Reconstitution Calculator allows you to calculate the volume of solvent required to reconstitute your vial.

  • Enter the mass of the reagent and the desired reconstitution concentration as well as the correct units
  • Click the “Calculate” button
  • The answer appears in the Volume (to add to vial) box
In vivo Formulation Calculator (Clear solution)
Step 1: Enter information below (Recommended: An additional animal to make allowance for loss during the experiment)
Step 2: Enter in vivo formulation (This is only a calculator, not the exact formulation for a specific product. Please contact us first if there is no in vivo formulation in the solubility section.)
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Calculation results

Working concentration mg/mL;

Method for preparing DMSO stock solution mg drug pre-dissolved in μL DMSO (stock solution concentration mg/mL). Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug.

Method for preparing in vivo formulation:Take μL DMSO stock solution, next add μL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O,mix and clarify.

(1) Please be sure that the solution is clear before the addition of next solvent. Dissolution methods like vortex, ultrasound or warming and heat may be used to aid dissolving.
             (2) Be sure to add the solvent(s) in order.

Clinical Trial Information
Title:Effect of Triple Versus Quadruple Therapy for Treating Helicobacter Pylori Infection
Status:Enrolling by invitation
updateDate:2026-05-07
Ctid:NCT07010744

Link: https://clinicaltrials.gov/ct2/show/NCT07010744

Conditions:Dyspepsia
Interventions:Quadruple therapy
Phase:N/A
Title:Comparative Effectiveness of Triple Versus Quadruple Therapy in the Treatment of Helicobacter Pylori Induced Gastritis
Status:Completed
updateDate:2025-12-31
Ctid:NCT07312721

Link: https://clinicaltrials.gov/ct2/show/NCT07312721

Conditions:Helicobacter Pylori Infection|Chronic Gastritis|Peptic Ulcer Disease
Interventions:Quadruple Therapy
Phase:Phase 4
Title:Effectiveness of Corticosteroid vs Ketorolac Shoulder Injections
Status:Withdrawn
updateDate:2024-11-15
Ctid:NCT04895280

Link: https://clinicaltrials.gov/ct2/show/NCT04895280

Conditions:Full-thickness Rotator Cuff Tear|Rotator Cuff Tendinitis
Interventions:Kenalog
Phase:Phase 4
View More

Title:Efficacy of Thyme Honey in The Management of Oral Aphthous Ulcers
Status:Not yet recruiting
updateDate:2024-05-20
Ctid:NCT06421038

Link: https://clinicaltrials.gov/ct2/show/NCT06421038

Conditions:Aphthous Stomatitis (Major) (Minor)|Treatment Compliance
Interventions:Kenalog
Phase:N/A
Title:Effectiveness of Corticosteroid vs. Ketorolac Shoulder Injections: A Prospective Double-Blinded Randomized Trial
Status:Terminated
updateDate:2023-12-14
Ctid:NCT04115644

Link: https://clinicaltrials.gov/ct2/show/NCT04115644

Conditions:Full Thickness Rotator Cuff Tear|Rotator Cuff Tendinitis
Interventions:Kenalog
Phase:Phase 4
Title:Glenohumeral Cortisone Injection
Status:Completed
updateDate:2023-09-26
Ctid:NCT04216017

Link: https://clinicaltrials.gov/ct2/show/NCT04216017

Conditions:Humeral Fractures
Interventions:Lidocaine
Phase:Phase 2
Title:Optimized-dose Amoxicillin Versus Standard-dose Amoxicillin for Quadruple Therapy in Helicobacter Pylori Eradication
Status:Completed
updateDate:2022-12-02
Ctid:NCT05635942

Link: https://clinicaltrials.gov/ct2/show/NCT05635942

Conditions:Helicobacter Pylori
Interventions:standard quadruple therapy
Phase:Phase 4
Title:Granulation Tissue Treatment: Silver Nitrate vs Kenalog vs Washcloth Abrasion
Status:Terminated
updateDate:2022-01-25
Ctid:NCT02519738

Link: https://clinicaltrials.gov/ct2/show/NCT02519738

Conditions:Other Abnormal Granulation Tissue Nos
Interventions:Kenalog (Triamcinolone)
Phase:Phase 3
Title:Steroid Injection vs. BioDRestore for Patients With Knee OA
Status:Completed
updateDate:2021-11-23
Ctid:NCT02767492

Link: https://clinicaltrials.gov/ct2/show/NCT02767492

Conditions:Knee Osteoarthritis
Interventions:Kenalog
Phase:N/A
Title:Comparison of Steroid Dosages on the Efficacy of Trochanteric Bursa Injection
Status:Completed
updateDate:2021-10-19
Ctid:NCT02126878

Link: https://clinicaltrials.gov/ct2/show/NCT02126878

Conditions:Bursitis
Interventions:Kenalog
Phase:N/A
Title:CANHelp Working Group Treatment Trials
Status:Completed
updateDate:2019-09-26
Ctid:NCT01967329

Link: https://clinicaltrials.gov/ct2/show/NCT01967329

Conditions:Helicobacter Pylori Infection
Interventions:Quadruple
Phase:Phase 4
Title:Onabotulinumtoxin A Versus Kenalog for Chronic Pelvic Pain
Status:Completed
updateDate:2019-07-24
Ctid:NCT02369068

Link: https://clinicaltrials.gov/ct2/show/NCT02369068

Conditions:Pelvic Pain
Interventions:Kenalog
Phase:N/A
Title:Empirical vs Tailored Therapy for H. Pylori Infection
Status:Unknown status
updateDate:2019-07-05
Ctid:NCT04006340

Link: https://clinicaltrials.gov/ct2/show/NCT04006340

Conditions:Helicobacter Pylori 23S rRNA Clarithromycin Resistance Mutation|Helicobacter Pylori Infection
Interventions:quadruple therapy
Phase:N/A
Title:Early Treatment for Acute ACL Tear
Status:Completed
updateDate:2018-12-05
Ctid:NCT01692756

Link: https://clinicaltrials.gov/ct2/show/NCT01692756

Conditions:Anterior Cruciate Ligament (ACL) Tears
Interventions:Placebo
Phase:Phase 2
Title:The Efficacy of Local Anesthetics to Reduce Shoulder Pain Post-Steroid Injections
Status:Terminated
updateDate:2018-10-16
Ctid:NCT02592629

Link: https://clinicaltrials.gov/ct2/show/NCT02592629

Conditions:Shoulder Pain
Interventions:Kenalog
Phase:Phase 4
Title:A Unique Regimen for Treatment of Helicobacter Pylori Infection
Status:Unknown status
updateDate:2018-04-10
Ctid:NCT03491995

Link: https://clinicaltrials.gov/ct2/show/NCT03491995

Conditions:Helicobacter Infections
Interventions:Classic treatment
Phase:Phase 3
Title:Concomitant, Sequential, and Standard Triple Therapy for H. Pylori Infection
Status:Completed
updateDate:2017-11-17
Ctid:NCT01769365

Link: https://clinicaltrials.gov/ct2/show/NCT01769365

Conditions:Helicobacter Pylori Infection
Interventions:7-day standard triple therapy
Phase:Phase 4
Title:A Study of Hyaluronan for the Treatment of Osteoarthritis in the Thumb
Status:Completed
updateDate:2017-07-07
Ctid:NCT00398866

Link: https://clinicaltrials.gov/ct2/show/NCT00398866

Conditions:Osteoarthritis
Interventions:Kenalog (triamcinolone; corticosteroid injection)
Phase:Phase 3
Title:Corticosteroid Injection Verses High Energy Extracorporeal Shock Wave Therapy for Lateral Epicondylitis
Status:Unknown status
updateDate:2015-11-24
Ctid:NCT02613455

Link: https://clinicaltrials.gov/ct2/show/NCT02613455

Conditions:Lateral Epicondylitis|Tennis Elbow
Interventions:lidocaine 1% (lidocaine HCl 20mg)
Phase:Phase 4
Title:Five Days Quadruple and Clarithromycin Containing Triple Therapy as Treatment for Helicobacter Pylori Eradication
Status:Completed
updateDate:2015-05-28
Ctid:NCT01306786

Link: https://clinicaltrials.gov/ct2/show/NCT01306786

Conditions:Helicobacter Pylori Infection
Interventions:Triple therapy
Phase:N/A
Title:Effects of Intra-articular Versus Subacromial Steroid Injections on Clinical Outcomes in Adhesive Capsulitis
Status:Withdrawn
updateDate:2015-02-27
Ctid:NCT00742846

Link: https://clinicaltrials.gov/ct2/show/NCT00742846

Conditions:Adhesive Capsulitis
Interventions:Lidocaine
Phase:N/A
Title:Quadruple Versus Sequential Therapy for Helicobacter Pylori Eradication
Status:Completed
updateDate:2013-01-04
Ctid:NCT01760824

Link: https://clinicaltrials.gov/ct2/show/NCT01760824

Conditions:Helicobacter Pylori Infection
Interventions:Quadruple therapy
Phase:N/A
Title:Study Of Combined VISUDYNE Therapy With Kenalog In CNV Secondary To Age-Related Macular Degeneration
Status:Completed
updateDate:2007-07-12
Ctid:NCT00140803

Link: https://clinicaltrials.gov/ct2/show/NCT00140803

Conditions:Age-Related Macular Degeneration
Interventions:Kenalog
Phase:Phase 2
Title:A phase II single arm, multi-centre trial of triamcinolone with a GnRH analog for castration resistant prostate cancer
Status:Completed
Date:2011-08-15
Eudractnumber:2010-022010-32

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2010-022010-32

Condition:Castration Resistent Prostate cancer
Phase:Phase 2
Title:Intraarticular injections for hip osteoarthritis: Steroid versus Hyaluronic acid: randomised controlled trial
Status:Prematurely Ended
Date:2009-11-18
Eudractnumber:2009-012442-23

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2009-012442-23

Condition:Osteoarthritis of hip joint
Phase:Phase 4
Title:An adaptive dose-ranging, multi-center, single-blind, double-dummy, active-controlled trial to determine the target dose of canakinumab (ACZ885) in the treatment of acute flares in gout patients who are refractory or contraindicated to NSAIDs and/or colchicine
Status:Completed, Prematurely Ended
Date:2008-10-09
Eudractnumber:2008-004666-61

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2008-004666-61

Condition:Acute gout (patients who are refractory or contraindicated to NSAIDs and/or colchicine)
Phase:Phase 2
Title:A prospective, multi-center, randomized, controlled, single-blinded study to evaluate the safety and efficacy of AdvaCoat Mx sinus gel for treatment of chronic rhinosinusitis without nasal polyps.
Status:Prematurely Ended
Date:2008-10-07
Eudractnumber:2008-004226-16

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2008-004226-16

Condition:Subjects with chronic rhinosinusitis without nasal polyps, who have not had previous sinus surgery might be eligible for participation in this trial.
Phase:Phase 2
Title:Examination of the efficacy of glycerol, two topical steroids and a topical immune modulator in experimentally induced skin irritation
Status:Completed
Date:2008-08-20
Eudractnumber:2008-001678-34

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2008-001678-34

Condition:Irritative contact dermatitis.
Phase:Phase 4
Title:PERIOPERATIVE INTRAVITREAL TRIAMCINOLONE IN PHAKOEMULSIFICATION FOR CONCURRENT CLINICALLY SIGNIFICANT DIABETIC MACULAR OEDEMA
Status:Prematurely Ended
Date:2008-07-25
Eudractnumber:2006-005400-14

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2006-005400-14

Condition:Diabetic Maculopathy: Clinically significant macular oedemaTo understand the effects of intravitreal triamcinolone (IVTA) in the treatment of clinically significant macular edema (CSME) in diabetics who have concurrent cataract which requires intervention.
Phase:Phase 4
Title:Triamcinolone acetonide to prevent PVR in eyes undergoing vitreoretinal surgery for open globe trauma
Status:Completed
Date:2008-06-06
Eudractnumber:2007-005138-35

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2007-005138-35

Condition:Proliferative vitreoretinopathy following open globe trauma.
Phase:Phase 4
Title:Is a single dose intramuscular (IM) triamcinolone acetonide injection more effective in treating symptomatic flare in established rheumatoid arthritis than equivalent dose of oral prednisolone?
Status:Completed
Date:2008-01-25
Eudractnumber:2007-006729-28

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2007-006729-28

Condition:The objective of this study is to compare the efficacy of equivalent doses of IM triamcinolone acetonide and oral prednisolone in controlling a symptomatic flare in patients with established RA.
Phase:Phase 4
Title:A Pilot Study to Examine the Safety and Efficacy of Posterior Juxtascleral Triamcinolone acetonide administration, in addition to Visudyne photoynamic therapy for predominantly Classic Choroidal Neovascularisation secondary to age related Macular degeneration: an open label randomised active controlled trial.
Status:Prematurely Ended
Date:2006-01-03
Eudractnumber:2005-002466-11

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2005-002466-11

Condition:Classic or predominantly classic age related macular degeneration
Phase:Phase 2
Title:A Pilot study investigating the use of Intravitreal Triamcinolone prior to macular laser for Clinically Significant Diabetic Macular Oedema
Status:GB - no longer in EU/EEA
Date:2005-06-30
Eudractnumber:2004-005043-97

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2004-005043-97

Condition:Macular oedema affects 29% of diabetic patients and is the main cause of visual impairment. Previous studies show that diffuse macular oedema carries a particularly poor prognosis despite laser photocoagulation.
Phase:Phase 4
Title:Randomised Controlled Trial Of Intravitreal Triamcinolone In Patients With Diabetic Macular Oedema Refractory To Laser Treatment
Status:Completed
Date:2005-06-02
Eudractnumber:2005-000397-45

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2005-000397-45

Condition:Diabetic macular oedema affecting vision and refractory to laser treatment
Phase:Phase 4
Title:A pilot study investigating the effects of a combination of local and systemic anti-inflammatory adjuncts in patients undergoing vitrectomy and silicone oil for established Proliferative Vitreoretinopathy.
Status:Completed
Date:2004-11-18
Eudractnumber:2004-001991-37

Link: https://www.clinicaltrialsregister.eu/ctr-search/search?query=2004-001991-37

Condition:Proliferative VitreoretinopathyThis is a scarring process that occurs in patients who have developed a retinal detachment. It is the primary cause of failure in retinal detachment surgery and occurs in 5-10% cases.
Phase:Phase 4

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