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Laser-Ranibizumab-Triamcinolone for Diabetic Macular Edema

Phase 3
Completed
Conditions
Diabetic Retinopathy
Diabetic Macular Edema
Interventions
Registration Number
NCT00444600
Lead Sponsor
Jaeb Center for Health Research
Brief Summary

The purpose of the study is to find out which is a better treatment for diabetic macular edema (DME): laser alone, laser combined with an intravitreal injection of triamcinolone, laser combined with an intravitreal injection of ranibizumab, or intravitreal injection of ranibizumab alone. At the present time, it is not known whether intravitreal steroid or anti-vascular endothelial growth factor (anti-VEGF) injections, with or without laser treatment, are better than just laser by itself. It is possible that one or both of the types of injections, with or without laser treatment, will improve vision more often than will laser without injections. However, even if better vision outcomes are seen with injections, side effects may be more of a problem with the injections than with laser. Therefore, this study is conducted to find out whether the benefits of the injections will outweigh the risks.

Detailed Description

Thus far the only demonstrated means to reduce the risk of vision loss from diabetic macular edema are laser photocoagulation, intensive glycemic control, and blood pressure control. Earlier studies have shown that photocoagulation, although effective in reducing the risk of moderate vision loss, can eventually result in retinal and retinal pigment epithelium atrophy resulting in loss of central vision, central scotomata, and decreased color vision. Consequently, many retinal specialists today tend to treat diabetic macular edema (DME) with lighter, less intense laser burns than was originally specified in the Early Treatment Diabetic Retinopathy Study (ETDRS). The additional unsatisfactory outcome from treatments with laser photocoagulation in a significant proportion of eyes with DME has prompted interest in other treatment modalities. One such treatment is pars plana vitrectomy. Studies suggest that vitreomacular traction may play a role in increased retinal vascular permeability, and that removal of the vitreous, or relief of mechanical traction with vitrectomy and membrane stripping may substantially improve macular edema and visual acuity. However, this treatment may be applicable only to a specific subset of eyes with a component of vitreomacular traction secondary to edema. Other treatment modalities such as pharmacologic therapy with oral protein kinase C inhibitors and intravitreal corticosteroids are under investigation.

The use of antibodies targeted at vascular endothelial growth factor (VEGF) is another treatment modality that needs to be further explored for its potential benefits. Increased VEGF levels have been demonstrated in the retina and vitreous of human eyes with diabetic retinopathy. VEGF, also knows as vascular permeability factor, has been shown to increase retinal vascular permeability in in vivo models. Therapy that inhibits VEGF, therefore, may represent a useful therapeutic modality which targets the underlying pathogenesis of diabetic macular edema. Ranibizumab is a promising anti-VEGF drug. Its efficacy and safety have been demonstrated in treatment of age-related macular degeneration. Reports of its use and that of other anti-VEGF drugs in DME have suggested sufficient benefit to warrant evaluation of efficacy and safety in a phase III trial. Corticosteroids, a class of substances with anti-inflammatory properties, have also been demonstrated to inhibit the expression of the VEGF gene. The Diabetic Retinopathy Clinical Research Network (DRCR.net) is currently conducting a phase III randomized clinical trial comparing focal photocoagulation to intravitreal corticosteroids (triamcinolone acetonide) for diabetic macular edema. However, even if triamcinolone or ranibizumab are proven to be efficacious, a major concern, based on clinical observations with intravitreal corticosteroids, is that DME will recur as the effect of the intravitreal drug wears off, necessitating repetitive injections long-term. Combining an intravitreal drug (triamcinolone or ranibizumab) with photocoagulation provides hope that one could get the short-term benefit of the intravitreal drug (decreased retinal thickening and decreased fluid leakage) and the long-term reduction in fluid leakage as a result of photocoagulation. In addition, it is possible that the worsening of macular edema immediately following focal photocoagulation, a known complication of this treatment, could be decreased if an intravitreal drug was present at the time of photocoagulation. This might result in an increased likelihood of vision improvement following photocoagulation and a decreased likelihood of vision loss.

This study is designed to determine if ranibizumab alone or ranibizumab added to laser photocoagulation is more efficacious than photocoagulation alone, and if so, to determine if combining ranibizumab with photocoagulation reduces the total number of injections needed to obtain these benefits. Furthermore, this study is designed to determine if combining photocoagulation with corticosteroids, the only other class of drugs currently being considered for treatment of DME, is efficacious in the population being enrolled.

Subjects will be randomly assigned to one of the following 4 groups:

1. Group A: Sham injection plus focal (macular) photocoagulation

2. Group B: 0.5 mg injection of intravitreal ranibizumab plus focal photocoagulation

3. Group C: 0.5 mg injection of intravitreal ranibizumab plus deferred focal photocoagulation

4. Group D: 4 mg intravitreal triamcinolone plus focal photocoagulation

In groups A, B and D, laser will be given 7-10 days after the initial injection at the time of the injection follow-up safety visit. During the first year, subjects are evaluated for retreatment every 4 weeks. The injection for group A is a sham and for groups B and C ranibizumab. For group D, a triamcinolone injection is given if one has not been given in the prior 15 weeks; otherwise a sham injection is given. For Groups A, B, and D, focal photocoagulation will be given 7 to 10 days later following each injection unless focal photocoagulation has been given in the past 15 weeks or no macular edema is present. In Years 2 and 3, subjects continue to be evaluated for retreatment every 4 weeks unless injections are discontinued due to failure. In that case, follow-up visits occur every 4 months and treatment is at investigator discretion.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
691
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
0.5mg Ranibizumab plus laserRanibizumab + laser-
0.5 mg Ranibizumab plus deferred laserRanibizumab + deferred laser-
Sham plus laserSham injection + laser-
4 mg Triamcinolone plus laserTriamcinolone Acetonide + laser-
Primary Outcome Measures
NameTimeMethod
Change in Visual Acuity From Baseline to 1 Year Among Eyes That Had Prior Treatment for Diabetic Macular Edemafrom baseline to 1 Year
Mean Change in Visual Acuity (Letters) From Baseline to 1 Year Adjusted for Baseline Visual Acuityfrom baseline to 1 Year

Change in best correct visual acuity letter score from baseline to one year as measured by a certified tester using an electronic visual acuity testing machine based on the Early Treatment Diabetic Retinopathy Study (ETDRS) method. A positive change denotes an improvement. Best value on the scale 97, worst 0.

Distribution of Change in Visual Acuity (Letters) From Baseline to 1 Yearfrom baseline to 1 Year

Change in best correct visual acuity letter score as measured by a certified tester using an electronic visual acuity testing machine based on the Early Treatment Diabetic Retinopathy Study (ETDRS) method.

Change in Visual Acuity From Baseline to 1 Year Among Eyes That Were Pseudophakic at Baselinefrom baseline to 1 Year
Change in Visual Acuity From Baseline to 1 Year Grouped by Baseline Visual Acuity Letter Scorefrom baseline to 1 Year

Change in best correct visual acuity letter score as measured by a certified tester using an electronic visual acuity testing machine based on the Early Treatment Diabetic Retinopathy Study (ETDRS) method. A positive change denotes an improvement. Best value on the scale 97, worst 0.

Change in Visual Acuity From Baseline to 1 Year Grouped by Optical Coherence Tomography Central Subfield Thicknessfrom baseline to 1 Year

Change in best correct visual acuity letter score from baseline to one year as measured by a certified tester using an electronic visual acuity testing machine based on the Early Treatment Diabetic Retinopathy Study (ETDRS) method. A positive change denotes an improvement. Best value on the scale 97, worst 0.

Change in Visual Acuity From Baseline to 1 Year Grouped by Diffuse vs. Focal Edema as Characterized by the Investigatorfrom baseline to 1 Year

Change in best correct visual acuity letter score from baseline to one year as measured by a certified tester using an electronic visual acuity testing machine based on the Early Treatment Diabetic Retinopathy Study (ETDRS) method. A positive change denotes an improvement. Best value on the scale 97, worst 0.

Change in Visual Acuity From Baseline to 1 Year Grouped by Diabetic Retinopathy Severityfrom baseline to 1 Year

Change in best correct visual acuity letter score from baseline to one year as measured by a certified tester using an electronic visual acuity testing machine based on the Early Treatment Diabetic Retinopathy Study (ETDRS) method. A positive change denotes an improvement. Best value on the scale 97, worst 0.

Secondary Outcome Measures
NameTimeMethod
Mean Change in Optical Coherence Tomography Retinal Volume From Baseline to 1 Yearfrom baseline to 1 Year
Change in Retinal Thickening of Central Subfield on Optical Coherence Tomography From Baseline to 1 Yearfrom baseline to 1 year

Negative change denotes an improvement.

Number of Injections in First Yearfrom baseline to 1 year

Maximum possible number of injections for each of the following groups: sham+prompt laser=13 sham injections;ranibizumab+prompt laser=13 ranibizumab injections; ranibizumab+deferred laser=13 ranibizumab injections; triamcinolone+prompt laser=4 triamcinolone injections and 9 sham injections.

Number of Laser Treatments Received Prior to the 1 Year Visit1 Year

One eye in the sham+prompt laser group did not receive laser until post 1-year due to an adverse event unrelated to study treatment. One eye in the triamcinolone+prompt laser did not receive laser until after 1-year due to missing 2 consecutive visits at the time of required laser treatment.

Percentage of Eyes Receiving Laser at the 48 Week Visit (%)1 Year
Mean Optical Coherence Tomography Retinal Volume at 1 Year1 Year

Trial Locations

Locations (49)

Retina Consultants of Southwest Florida

🇺🇸

Fort Myers, Florida, United States

Southeastern Retina Associates, P.C.

🇺🇸

Knoxville, Tennessee, United States

Elman Retina Group, P.A.

🇺🇸

Baltimore, Maryland, United States

Wilmer Eye Institute at Johns Hopkins

🇺🇸

Baltimore, Maryland, United States

Ophthalmic Consultants of Boston

🇺🇸

Boston, Massachusetts, United States

University of Washington Medical Center

🇺🇸

Seattle, Washington, United States

Retina Consultants of Delmarva, P.A.

🇺🇸

Salisbury, Maryland, United States

Paducah Retinal Center

🇺🇸

Paducah, Kentucky, United States

Medical Associates Clinic, P.C.

🇺🇸

Dubuque, Iowa, United States

Carolina Retina Center

🇺🇸

Columbia, South Carolina, United States

Case Western Reserve University

🇺🇸

Cleveland, Ohio, United States

Retina and Vitreous Associates of Kentucky

🇺🇸

Lexington, Kentucky, United States

Charlotte Eye, Ear, Nose and Throat Assoc., PA

🇺🇸

Charlotte, North Carolina, United States

Palmetto Retina Center

🇺🇸

Columbia, South Carolina, United States

Retina Research Center

🇺🇸

Austin, Texas, United States

Retina-Vitreous Surgeons of Central New York, PC

🇺🇸

Syracuse, New York, United States

Vitreoretinal Consultants

🇺🇸

Houston, Texas, United States

Eyesight Ophthalmic Services, PA

🇺🇸

Portsmouth, New Hampshire, United States

University of Wisconsin-Madison, Dept of Ophthalmology/Retina Service

🇺🇸

Madison, Wisconsin, United States

Texas Retina Associates

🇺🇸

Lubbock, Texas, United States

The New York Eye and Ear Infirmary/Faculty Eye Practice

🇺🇸

New York, New York, United States

Casey Eye Institute

🇺🇸

Portland, Oregon, United States

Raj K. Maturi, M.D., P.C.

🇺🇸

Indianapolis, Indiana, United States

Retina Center, PA

🇺🇸

Minneapolis, Minnesota, United States

University of Florida College of Med., Department of Ophthalmology

🇺🇸

Jacksonville, Florida, United States

John-Kenyon American Eye Institute

🇺🇸

New Albany, Indiana, United States

Retina Northwest, PC

🇺🇸

Portland, Oregon, United States

Sall Research Medical Center

🇺🇸

Artesia, California, United States

Loma Linda University Health Care, Dept. of Ophthalmology

🇺🇸

Loma Linda, California, United States

Retina-Vitreous Associates Medical Group

🇺🇸

Beverly Hills, California, United States

Southern California Desert Retina Consultants, MC

🇺🇸

Palm Springs, California, United States

Bay Area Retina Associates

🇺🇸

Walnut Creek, California, United States

California Retina Consultants

🇺🇸

Santa Barbara, California, United States

Southeastern Retina Associates, PC

🇺🇸

Kingsport, Tennessee, United States

West Texas Retina Consultants P.A.

🇺🇸

Abilene, Texas, United States

Retina and Vitreous of Texas

🇺🇸

Houston, Texas, United States

Retina Vitreous Consultants

🇺🇸

Fort Lauderdale, Florida, United States

Retina Associates of Cleveland, Inc.

🇺🇸

Beachwood, Ohio, United States

Penn State College of Medicine

🇺🇸

Hershey, Pennsylvania, United States

Central Florida Retina Institute

🇺🇸

Lakeland, Florida, United States

Southeast Retina Center, P.C.

🇺🇸

Augusta, Georgia, United States

Illinois Retina Associates

🇺🇸

Joliet, Illinois, United States

University of Pennsylvania Scheie Eye Institute

🇺🇸

Philadelphia, Pennsylvania, United States

Retina Consultants

🇺🇸

Providence, Rhode Island, United States

University of California, Irvine

🇺🇸

Irvine, California, United States

Joslin Diabetes Center

🇺🇸

Boston, Massachusetts, United States

Medical College of Wisconsin

🇺🇸

Milwaukee, Wisconsin, United States

University of North Carolina, Dept of Ophthalmology

🇺🇸

Chapel Hill, North Carolina, United States

Wake Forest University Eye Center

🇺🇸

Winston-Salem, North Carolina, United States

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