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Sorbinil Retinopathy Trial (SRT)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT00000159
Recruitment Status : Completed
First Posted : September 24, 1999
Last Update Posted : June 24, 2005
Information provided by:
National Eye Institute (NEI)

Brief Summary:
To evaluate the safety and efficacy of the investigational drug sorbinil, an aldose reductase inhibitor, in preventing the development of diabetic retinopathy and neuropathy in persons with insulin-dependent diabetes.

Condition or disease Intervention/treatment Phase
Diabetic Retinopathy Diabetes Mellitus Drug: Sorbinil Phase 3

Detailed Description:

During the last two decades, vision researchers have studied intensively the role of the enzyme aldose reductase (AR) in diabetic cataract and in other diabetic complications. The potentially damaging effects of AR in diabetes were first discovered in the lens fiber cells. In these cells, the enzyme catalyzes the reduction of high levels of glucose to sorbitol through the polyol pathway and initiates a sequence of events that eventually results in opacification of the lens. Because sorbitol (a sugar alcohol) and fructose (a subsequent product of glucose metabolism) cannot readily diffuse across cell membranes, they become trapped in lens fiber cells. There they accumulate at unusually high levels and exert a significant osmotic stress, causing an influx of water and swelling of the lens fibers. Major electrolytic and osmotic changes then occur that lead to lens opacity.

More recently, the detection of AR in the pericytes of retinal capillaries -- cells that are involved very early in the evolution of diabetic retinopathy -- suggests that this enzyme may also play a role in the pathogenesis of this disorder. Scientists now know that AR is present in nerve tissue, and they speculate that in diabetes it induces the depletion of myo -inositol, which leads to the lessening of nerve conduction velocity in diabetic neuropathy.

Chemicals that inhibit aldose reductase have proved effective in preventing damage to the lens, in preventing thickening of retinal capillary basement membranes in diabetic animals, and in improving nerve conduction velocity values in patients with diabetic neuropathy. Therefore, it is possible that AR inhibitors also may be able to prevent, delay, or halt the development or progression of diabetic retinopathy.

To test this hypothesis, an AR inhibitor developed by Pfizer Inc., sorbinil, was studied in this clinical trial. (Other AR inhibitors underwent study in clinical trials sponsored by Ayerst and Alcon.) Initially, 402 patients were randomized into the double-masked treatment period using a dosage schedule of one 250-mg tablet daily. In 1985, recruitment was voluntarily halted by Pfizer because of several serious hypersensitivity reactions among patients taking sorbinil in clinical trials in the United States and Europe. In November 1985, recruitment resumed, using a titrated dosage schedule of 25 mg daily for 2 weeks, followed by 75 mg daily for 2 weeks, then 250 mg daily for the duration. A total of 497 patients participated in the study.

Followup visits were scheduled weekly for the first 4 weeks, monthly for the next 2 months, and every 3 months thereafter. For patients assigned to the titration protocol, additional visits were made at weeks 5 and 6. A complete history was recorded and a physical examination was conducted every 15 months; electrocardiogram was recorded every 6 months. In addition, patients were cautioned to note any signs of hypersensitivity.

Efficacy visits, scheduled at 9-month intervals after the first visit at 12 months, included fundus photographs, visual acuity examinations according to the Early Treatment Diabetic Retinopathy Study (ETDRS), red blood cell sorbitol measure, and assessment of coronary risk factor classification.

The Sorbinil Retinopathy Trial (SRT) was a unique collaboration between private industry and the Federal government in designing, funding, and conducting a multicenter, randomized clinical trial. Pfizer Inc. supported 10 of the 11 participating Clinical Centers, provided the medication, and funded the Data Coordinating Center and Fundus Photograph Reading Center. The National Eye Institute funded the Policy, Data, and Safety Monitoring Committee and its own participating Clinical Center.

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Study Type : Interventional  (Clinical Trial)
Allocation: Randomized
Masking: Double
Primary Purpose: Treatment
Study Start Date : August 1983

Resource links provided by the National Library of Medicine

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years to 56 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Men and women eligible for the SRT had diabetes for 1 to 15 years and were between ages 18 and 56 at the time of enrollment. They had begun taking insulin before their 41st birthday. Their hemoglobin A1c value was within the diabetic range. On retinal examination, they showed no evidence of or only very mild retinopathy, with no more than five microaneurysms per eye. Women were postmenopausal, sterile, or had an IUD in place.
Layout table for additonal information Identifier: NCT00000159    
Other Study ID Numbers: NEI-61
First Posted: September 24, 1999    Key Record Dates
Last Update Posted: June 24, 2005
Last Verified: October 1999
Additional relevant MeSH terms:
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Retinal Diseases
Diabetic Retinopathy
Eye Diseases
Diabetic Angiopathies
Vascular Diseases
Cardiovascular Diseases
Diabetes Complications
Diabetes Mellitus
Endocrine System Diseases