Progression of Diabetic Retinopathy Post Bariatric Surgery (BS)

Sponsor
NYU Langone Health (Other)
Overall Status
Terminated
CT.gov ID
NCT01393873
Collaborator
(none)
2
1
12
0.2

Study Details

Study Description

Brief Summary

Studies conducted assessing diabetic eye disease have shown a progression of diabetic retinopathy with rapid improvement of glycemic control during pregnancy and in patients with type 1 diabetes. It is also well documented that bariatric surgery may result in rapid improvement of glycemic control in obese patients with type 2 diabetes. To our knowledge the progression of diabetic eye disease seen in pregnancy and type 1 diabetes has not been studied in obese type 2 diabetics undergoing bariatric surgery. To this end, this study will examine the effects of rapid glycemic control which is seen in type 2 diabetics following bariatric surgery on the progression of diabetic retinopathy.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Participants will be referred from the Department of Bariatric Surgery at NYU. The investigators plan to enroll 50 patients in this pilot study.

    A baseline eye exam will be conducted prior to surgery. Data, such as preoperative HbA1c level, weight, BMI, duration and control of diabetes, current medication regimen, and the grade of retinopathy will be noted. Study participants will have a baseline eye exam within three months of the scheduled surgery, followed by regular follow-up visits at 3 months, 6 months, 9 months, and 1 year. At each visit the following measures will be assessed: (1) weight, (2) blood pressure, (3) glycemic control as assessed by HbA1C, (4)level of retinopathy, and (5) visual acuity using the EDTRS acuity chart.

    The eye examinations will consist of a measure of best-corrected visual acuity, slit lamp examination to assess pressure, and a dilated funduscopic examination to determine the presence and/or level of retinopathy. The level of retinopathy will be characterized as:

    (0)None, (1) Mild, (2) Moderate, (3) Severe, and (4) Proliferative. In addition, the presence or absence of cystoid macular edema (CME) will be noted as (a) no CME or (b) CME present.

    At the initial visit, a baseline questionnaire will be given to participants to gather background information on demographics and pertinent medical history. During each follow up visit, an additional questionnaire will be given to monitor changes in factors such as medications, blood pressure, and weight that may occur after bariatric surgery.

    HbA1c measurements will be checked every 3 months in accordance with current standard of care recommendations. Due to established evidence of rapid improvement in glycemic control shortly after bariatric surgery, it is essential that the investigators have this lab data and perform funduscopic examinations at these intervals, to monitor improvement in glycemic control ascertain associations between changes in HbA1c levels and progression of retinopathy.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    2 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    The Effect of Bariatric Surgery on the Progression of Diabetic Retinopathy
    Study Start Date :
    Jul 1, 2011
    Actual Primary Completion Date :
    Jul 1, 2012
    Actual Study Completion Date :
    Jul 1, 2012

    Arms and Interventions

    Arm Intervention/Treatment
    Bariatric surgery pts with Type 2 DM

    Primary bariatric surgery pts with Type 2 DM

    Outcome Measures

    Primary Outcome Measures

    1. rapid changes in the level of retinopathy [12 months]

      whether rapid changes in the level of retinopathy do or do not occur in the transition period following surgery, where weight loss may be rapid causing improvement in insulin resistance and glycemic control.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All patients, both male and female greater than 18 years old, with type 2 diabetes referred for bariatric surgery.
    Exclusion Criteria:
    • Patients will not be included in the study if they are pregnant, have HIV or any retinal vascular diseases (e.g. BRVO, CRVO) besides retinopathy.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 NYU SOM New York New York United States 10016

    Sponsors and Collaborators

    • NYU Langone Health

    Investigators

    • Principal Investigator: Ann Danoff, M.D., NYU SOM

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Heekoung A Youn, Research coordinator, NYU Langone Health
    ClinicalTrials.gov Identifier:
    NCT01393873
    Other Study ID Numbers:
    • R10-02084
    First Posted:
    Jul 13, 2011
    Last Update Posted:
    Sep 27, 2012
    Last Verified:
    Sep 1, 2012
    Keywords provided by Heekoung A Youn, Research coordinator, NYU Langone Health
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 27, 2012