A Single-Center Trial of Intravitreous Injections of Macugen (Pegaptanib Sodium) Given at Least 7 Days Before Vitrectomy Secondary To Tractional Retinal Detachment in Proliferative Diabetic Retinopathy
Completed · Phase 1
Conditions studied: PDR
In brief
Primary objective of this trial will be to evaluate the safety and efficacy of intravitreal injections of Macugen (pegaptanib sodium) when given at least 7-14 days prior to vitrectomy in subjects with tractional retinal detachment (with or withoutmacular involvement) secondary to proliferative diabetic retinopathy. Secondary objective is to evaluate regression of neovascularization and progression of macular traction utilizing OCT and fundus photographs.
Key facts
- Study ID
- NCT01487070
- Run by
- Retina Institute of Hawaii
- People needed
- 5
- Starts
- 2011-04-01
- Expected to finish
- 2011-07-01
- Last updated by the study team
- 2011-12-07
Who can join
Age: any, up to 75. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects of either gender aged 75 years or below diagnosed with tractional retinal detachment secondary to proliferative diabetic retinopathy.
You may not qualify if…
- Subjects with vitreous hemorrhage obscuring the posterior pole will be excluded.
Where it is running
- Retina Institute of Hawaii — Honolulu, Hawaii, United States
Full record on ClinicalTrials.gov
Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.