Clinical Trial

Early Vitrectomy vs PRP in Early Proliferative Diabetic Retinopathy

Recruiting
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Record status
This record was last updated May 14, 2026 (before its estimated June 10, 2026 completion). Its status may not reflect the trial's current state.
Summary
The goal of this clinical trial is to learn whether early microincision vitrectomy surgery (MIVS) can improve retinal neovascularization outcomes compared to standard pan-retinal photocoagulation (PRP) in patients with early proliferative diabetic retinopathy (PDR). It will also evaluate the safety and functional outcomes of early surgical intervention in this population. The main questions it aims to answer are: Does early MIVS increase the proportion of eyes achieving complete regression of retinal neovascularization at 12 months? Does early MIVS improve visual and functional outcomes, including visual acuity and visual field, compared to PRP? Researchers will compare early MIVS combined with peripheral scatter photocoagulation to standard PRP to determine whether early surgical intervention leads to better regression of neovascularization and improved clinical outcomes. Participants will: Receive either MIVS with peripheral photocoagulation or standard PRP Undergo retinal imaging assessments including fundus fluorescein angiography (FFA) or optical coherence tomography angiography (OCTA) Complete follow-up visits over 12 months, including visual acuity testing, visual field testing, and optical coherence tomography (OCT) imaging Be monitored for the occurrence of vitreous hemorrhage and other clinical outcomes
Trial Details
NCT Number NCT07586787
Lead Sponsor Xiamen Ophthalmology Center Affiliated to Xiamen University
Collaborators: Jiangsu Provincial People's Hospital, Peking University People's Hospital, Henan Provincial People's Hospital, Nanjing Medical University, The First Affiliated Hospital of Dalian Medical University
Conditions Proliferative Diabetic Retinopathy (PDR)
Enrollment 100 participants
Start Date 2025-01-01
Primary Completion 2026-06-10 (estimated)
Study Completion 2026-06-10 (estimated)
Updated on ClinicalTrials.gov 2026-05-14