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A Multicentre Randomised Clinical Trial of Laser Treatment Plus Intravitreal Triamcinolone for Diabetic Macular Oedema

Primary Purpose

Diabetic Macular Oedema

Status
Completed
Phase
Phase 2
Locations
Australia
Study Type
Interventional
Intervention
Triamcinolone acetate
Sponsored by
University of Sydney
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Macular Oedema focused on measuring Diabetic macular oedema, Triamcinolone acetate, Intravitreal injection, Clinical trial, Laser treatment

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age >= 18 years Diagnosis of diabetes mellitus types 1 or 2 Diabetic macular oedema affecting the fovea in one or both eyes (phakic or pseudophakic) for which laser treatment is indicated in the opinion of the investigator Best corrected visual acuity of 19-68 letters (6/12 -6/120) Definite macular oedema on clinical examination involving the centre of the macula Retinal thickness > 250 micron in central 1mm subfield on OCT Investigator is comfortable deferring macular laser treatment for 6 weeks Exclusion Criteria: Glaucoma which is uncontrolled or is controlled but with glaucomatous field defects Loss of vision due to other causes (e.g. age related macular degeneration, myopic macular degeneration, retinal vein occlusion) Macular oedema due to other causes including vitreous traction An ocular condition that would prevent visual acuity improvement despite resolution of oedema (such as foveal atrophy) Previous treatment IVTA within 6 months or with peribulbar TA within 3 months Cataract surgery within the last 6 months Retinal laser treatment within the last 4 months High risk PDR at baseline or laser therapy cannot be delayed for 6 weeks on retina History of herpes viral disease in study eye Media opacity including cataract that already precludes adequate macular photography and laser treatment, or cataract that is likely to preclude an adequate view within 2 years Known allergies to triamcinolone acetate Patient is already receiving systemic steroid treatment Intercurrent severe disease such as septicemia, any condition which would affect follow-up or photographic documentation (e.g. geographical, psycho-social) History of chronic renal failure requiring dialysis or renal transplant Blood pressure >180/110 mmHg

Sites / Locations

  • Save Sight Institute, Sydney/Sydney Eye Hospital Campus, University of Sydney

Outcomes

Primary Outcome Measures

The proportion of eyes showing an improvement of visual acuity by 10 letters on a LogMAR chart compared with the pre-injection level 24 months after treatment
At 24 months, improvement of ≥10 LogMAR letters was seen in 15/42 (36%) eyes treated with IVTA plus laser compared with 7/42 (17%) eyes treated with laser only (p=0.047, odds ratio 2.79, 95% CI, 1.01, 7.67).

Secondary Outcome Measures

Number of laser treatments required for the treatment of macular oedema during the course of the study.
At least 1 retreatment was required in the second year of the study in 29/42 (69%) of IVTA plus laser treated eyes compared with 19/42 (45%) laser only eyes (p=0.187).
Change in retinal thickness demonstrated on optical coherence tomography (OCT)
There was no difference in the mean CMT (346.8μm ± 114.9SD vs 372.6μm ± 154.2SD, comparing IVTA plus laser vs laser only, p=0.349) or mean logMAR visual acuity (56.1 ± 15.7SD vs 54.5 ± 16.1SD letters, p=0.439).
The incidence of moderate or severe side effects related to the procedure of intravitreal injection or related to the drug
Cataracts were removed from 17/28 (61%) of phakic IVTA plus laser-treated eyes vs. 0/27 (0%) laser only eyes (p<0.001). Treatment for elevated intraocular pressure was required in 27/42 (64%) of the IVTA plus laser eyes compared with 10/42 (24%) laser only eyes (p<0.001)

Full Information

First Posted
September 6, 2005
Last Updated
June 21, 2010
Sponsor
University of Sydney
Collaborators
The University of Western Australia, University of Melbourne, Marsden Eye Specialists
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1. Study Identification

Unique Protocol Identification Number
NCT00148265
Brief Title
A Multicentre Randomised Clinical Trial of Laser Treatment Plus Intravitreal Triamcinolone for Diabetic Macular Oedema
Official Title
Phase II/III Multicentre Randomised Clinical Trial of Laser Treatment Plus 4 mg Intravitreal Triamcinolone Injection to Reduce Diabetic Macular Oedema
Study Type
Interventional

2. Study Status

Record Verification Date
November 2005
Overall Recruitment Status
Completed
Study Start Date
April 2005 (undefined)
Primary Completion Date
May 2009 (Actual)
Study Completion Date
May 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
University of Sydney
Collaborators
The University of Western Australia, University of Melbourne, Marsden Eye Specialists

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This study is likely to identify an improved and economical treatment for diabetic macular oedema, one of the commonest causes of blindness both in Australia and the rest of the world.The specific aims of the study are to test the following hypotheses: That intravitreal triamcinolone followed by laser treatment results in a greater improvement in visual acuity than placebo followed by laser treatment of eyes with macular oedema secondary to diabetes; That intravitreal triamcinolone followed by laser treatment results in greater degree of resolution of macular oedema than placebo followed by laser treatment of eyes with macular oedema secondary to diabetes; That intravitreal triamcinolone followed by laser treatment results in a reduced requirement for further laser treatment to control diabetic macular oedema than placebo followed by laser treatment; That intravitreal triamcinolone followed laser has a manageable and acceptable safety profile in eyes with diabetic macular edema.
Detailed Description
A 25 fold increase in the risk of going blind on diagnosis of diabetes is one of the most daunting threats that people with diabetes face. Stimulated by several uncontrolled, anecdotal reports, we are already conducting a randomized clinical trial of intravitreal triamcinolone for the treatment of diabetic macular edema which is refractory to conventional laser treatment. The analysis of the 3 month data from this study has already unequivocally demonstrated that the treatment very significantly reduces or eliminates macular oedema in the short term and results in improved visual acuity. Thus intravitreal triamcinolone may represent the most significant development in the prevention of blindness in people with diabetes since the introduction of laser treatment. It is also a highly cost-effective intervention that can be administered by general ophthalmologists. The next question to be answered, which will be addressed directly by the present study, is whether there is a significant, synergistic beneficial effect when intravitreal steroids are combined with current therapy (laser). This study represents the second major project to be undertaken by the Australian Retinal Collaboration (ARC). The ARC aims to set the highest attainable standards for investigator-initiated clinical research in retinal diseases in Australia. Having enrolled and treated more than the target of 120 patients, we are currently completing an RCT of laser induced chorioretinal anastomosis for central retinal vein occlusion, an innovative Australian concept for a severe and otherwise untreatable disease. The proposed study is likely to identify an improved and economical treatment for one of the commonest causes of blindness both in Australia and the rest of the world. Intravitreal triamcinolone is also an intervention which has generated intense interest internationally, and one for which members of the ARC are acknowledged pioneers. Successful implementation of the study proposed, which is feasible, is highly likely to have an immediate and direct effect on the prevention of vision impairment and blindness in people with diabetes

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Macular Oedema
Keywords
Diabetic macular oedema, Triamcinolone acetate, Intravitreal injection, Clinical trial, Laser treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
54 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Triamcinolone acetate
Other Intervention Name(s)
Kenacort 40©
Intervention Description
Eyes assigned to IVTA received an intravitreal injection of 0.1 ml of Kenacort 40© [40mg/ml triamcinolone acetonide, Bristol-Myers Squibb pharmaceuticals, Australia] on the day of the baseline visual acuity measurement under sterile conditions in a minor procedures area as an outpatient procedure. Eyes assigned to placebo were prepared in the same way but had the barrel of the syringe without a needle pushed firmly against the eye to simulate an injection.
Primary Outcome Measure Information:
Title
The proportion of eyes showing an improvement of visual acuity by 10 letters on a LogMAR chart compared with the pre-injection level 24 months after treatment
Description
At 24 months, improvement of ≥10 LogMAR letters was seen in 15/42 (36%) eyes treated with IVTA plus laser compared with 7/42 (17%) eyes treated with laser only (p=0.047, odds ratio 2.79, 95% CI, 1.01, 7.67).
Time Frame
24 month
Secondary Outcome Measure Information:
Title
Number of laser treatments required for the treatment of macular oedema during the course of the study.
Description
At least 1 retreatment was required in the second year of the study in 29/42 (69%) of IVTA plus laser treated eyes compared with 19/42 (45%) laser only eyes (p=0.187).
Time Frame
24 month
Title
Change in retinal thickness demonstrated on optical coherence tomography (OCT)
Description
There was no difference in the mean CMT (346.8μm ± 114.9SD vs 372.6μm ± 154.2SD, comparing IVTA plus laser vs laser only, p=0.349) or mean logMAR visual acuity (56.1 ± 15.7SD vs 54.5 ± 16.1SD letters, p=0.439).
Time Frame
24 month
Title
The incidence of moderate or severe side effects related to the procedure of intravitreal injection or related to the drug
Description
Cataracts were removed from 17/28 (61%) of phakic IVTA plus laser-treated eyes vs. 0/27 (0%) laser only eyes (p<0.001). Treatment for elevated intraocular pressure was required in 27/42 (64%) of the IVTA plus laser eyes compared with 10/42 (24%) laser only eyes (p<0.001)
Time Frame
24 month

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >= 18 years Diagnosis of diabetes mellitus types 1 or 2 Diabetic macular oedema affecting the fovea in one or both eyes (phakic or pseudophakic) for which laser treatment is indicated in the opinion of the investigator Best corrected visual acuity of 19-68 letters (6/12 -6/120) Definite macular oedema on clinical examination involving the centre of the macula Retinal thickness > 250 micron in central 1mm subfield on OCT Investigator is comfortable deferring macular laser treatment for 6 weeks Exclusion Criteria: Glaucoma which is uncontrolled or is controlled but with glaucomatous field defects Loss of vision due to other causes (e.g. age related macular degeneration, myopic macular degeneration, retinal vein occlusion) Macular oedema due to other causes including vitreous traction An ocular condition that would prevent visual acuity improvement despite resolution of oedema (such as foveal atrophy) Previous treatment IVTA within 6 months or with peribulbar TA within 3 months Cataract surgery within the last 6 months Retinal laser treatment within the last 4 months High risk PDR at baseline or laser therapy cannot be delayed for 6 weeks on retina History of herpes viral disease in study eye Media opacity including cataract that already precludes adequate macular photography and laser treatment, or cataract that is likely to preclude an adequate view within 2 years Known allergies to triamcinolone acetate Patient is already receiving systemic steroid treatment Intercurrent severe disease such as septicemia, any condition which would affect follow-up or photographic documentation (e.g. geographical, psycho-social) History of chronic renal failure requiring dialysis or renal transplant Blood pressure >180/110 mmHg
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mark C Gillies, MBBS, PhD
Organizational Affiliation
Save Sight Institute, Deaprtment of Clinical Ophthalmology, University of Sydney
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ian L McAllister, MBBS
Organizational Affiliation
Lions Eye Institute, The University of Western Australia
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tien Wong, MBBS, PhD
Organizational Affiliation
Royal Victoria Eye & Ear Hospital, Department of Ophthalmology, University of Melbourne
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jennifer Arnold, MBBS
Organizational Affiliation
Marsden Eye Centre Parramatta
Official's Role
Principal Investigator
Facility Information:
Facility Name
Save Sight Institute, Sydney/Sydney Eye Hospital Campus, University of Sydney
City
Sydney
State/Province
New South Wales
ZIP/Postal Code
2000
Country
Australia

12. IPD Sharing Statement

Citations:
PubMed Identifier
15522370
Citation
Sutter FK, Simpson JM, Gillies MC. Intravitreal triamcinolone for diabetic macular edema that persists after laser treatment: three-month efficacy and safety results of a prospective, randomized, double-masked, placebo-controlled clinical trial. Ophthalmology. 2004 Nov;111(11):2044-9. doi: 10.1016/j.ophtha.2004.05.025.
Results Reference
background
PubMed Identifier
15860283
Citation
Larsson J, Zhu M, Sutter F, Gillies MC. Relation between reduction of foveal thickness and visual acuity in diabetic macular edema treated with intravitreal triamcinolone. Am J Ophthalmol. 2005 May;139(5):802-6. doi: 10.1016/j.ajo.2004.12.054.
Results Reference
background
PubMed Identifier
18599569
Citation
Wickremasinghe SS, Rogers SL, Gillies MC, Zhu M, Wong TY. Retinal vascular caliber changes after intravitreal triamcinolone treatment for diabetic macular edema. Invest Ophthalmol Vis Sci. 2008 Nov;49(11):4707-11. doi: 10.1167/iovs.08-1678. Epub 2008 Jul 3.
Results Reference
result
PubMed Identifier
17712074
Citation
Mohamed Q, Gillies MC, Wong TY. Management of diabetic retinopathy: a systematic review. JAMA. 2007 Aug 22;298(8):902-16. doi: 10.1001/jama.298.8.902.
Results Reference
result
PubMed Identifier
17405800
Citation
Gillies MC, Islam FM, Zhu M, Larsson J, Wong TY. Efficacy and safety of multiple intravitreal triamcinolone injections for refractory diabetic macular oedema. Br J Ophthalmol. 2007 Oct;91(10):1323-6. doi: 10.1136/bjo.2006.113167. Epub 2007 Apr 3.
Results Reference
result
PubMed Identifier
20019369
Citation
Gillies MC, McAllister IL, Zhu M, Wong W, Louis D, Arnold JJ, Wong TY. Pretreatment with intravitreal triamcinolone before laser for diabetic macular edema: 6-month results of a randomized, placebo-controlled trial. Invest Ophthalmol Vis Sci. 2010 May;51(5):2322-8. doi: 10.1167/iovs.09-4400. Epub 2009 Dec 17.
Results Reference
result

Learn more about this trial

A Multicentre Randomised Clinical Trial of Laser Treatment Plus Intravitreal Triamcinolone for Diabetic Macular Oedema

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