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Clinical Trial Summary

Currently, diabetic macular edema is treated is through injection of a medications such as off-label bevacizumab, which decreases the swelling in the retina. These injections are sometimes required monthly until the condition is controlled. Recently, there have been some new FDA approved treatments using laser that decrease the swelling. These approximately ten minute treatments do not require injections and don't cause permanent damage to the eye, and they may decrease the number of injections one needs to get to treat diabetic macular edema (DME).

The purpose of this randomized clinical trial is to determine whether subvisible laser in combination with intravitreal bevacizumab is non-inferior compared to current standard of care (intravitreal bevacizumab alone) in achieving favorable outcomes for visual acuity, mean macular thickness, and patient quality of life, and has fewer needed intravitreal bevacizumab injections throughout the course of the 12 month study period.


Clinical Trial Description

The patient is randomized into one of two study groups described below.

- Group 1: Intravitreal bevacizumab (IVB) will be administered at the first 3 monthly visits and subvisible laser treatment will be administered at the first visit. The the patient will undergo monthly visits, as he/she would with standard of care treatment, allowing for retreatment with monthly IVB and laser treatment every 3 months if defined retreatment criteria are met, as determined by a physician.

- Group 2: Intravitreal bevacizumab (IVB) will be administered at the first 3 monthly visits. The patient will then undergo monthly exams, as he or she would with standard of care treatment, allowing for retreatment with monthly IVB if defined retreatment criteria are met, as determined by a physician. The patient may also undergo sham laser treatment (he/she will be placed in front of laser but no laser will be activated) so that the patient isn't made aware of which treatment group he/she is a part of.

Other data that will be collected throughout the study at monthly examinations:

- Monthly Snellen Visual acuity test

- Monthly spectral-domain optical coherence tomography (SD-OCT) imaging using standard clinic protocol monthly

- Standard clinic diabetic montage Fundus photos at months 0,6,12

- Fluorescein angiography at months 0, 6, 12

The subjects' visit schedules will be the same as for routine standard of care for the IVB injection procedure. There are no additional appointments for this study.

All study procedures will be done at San Francisco General Hospital ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02229175
Study type Interventional
Source University of California, San Francisco
Contact
Status Withdrawn
Phase Phase 2/Phase 3
Start date January 1, 2021
Completion date January 1, 2027

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