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NCT02036632 · ClinicalTrials.gov registry record · Phase 1
Eye Patch Therapy for Central Serous Retinopathy (CSR)
A Phase 1 study, sponsored by Washington University School of Medicine.
- Completed
- Registry status
- Phase 1
- Development phase
- 12
- Enrollment target
NCT02036632: Completed Phase 1 study, sponsored by Washington University School of Medicine.
NCT02036632 is a Phase 1 study that has completed, run by Washington University School of Medicine. The registered enrollment target is 12 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT02036632, a Phase 1 study, has completed, sponsored by Washington University School of Medicine.
- COMPLETED
- Registry status
- Phase 1
- Development phase
- 12 participants
- Enrollment target
Study Summary
First, this study will investigate the viability of 24-hour eye patching as a potential treatment modality for CSR. Second, this study will assess a potential physiologic explanation for CSR, namely if inhibition of photic stimulation of the diseased retina will aid in ameliorating disease severity and disease duration.
Primary Outcome
This study is a prospective control trial that will compare 24-hour eye patch therapy with the current standard of care in patients with central serous retinopathy (CSR).
Interventions
- DEVICE Eye Patching
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 12 participants |
| Start Date | 2012-11 |
| Est. Completion | 2015-01 |
| Phase | Phase 1 |
What the finished NCT02036632 record still lists
NCT02036632 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 12 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (80% lower).
The record links to 0 conditions, and to 1 intervention - of which Eye Patching is the first listed.
NCT02036632 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT02036632 about?
NCT02036632 is a clinical study titled "Eye Patch Therapy for Central Serous Retinopathy (CSR)". First, this study will investigate the viability of 24-hour eye patching as a potential treatment modality for CSR. Second, this study will assess a potential physiologic explanation for CSR, namely if inhibition of photic stimulation of the diseased retina will aid in ameliorating disease severity ...
What is the current status of trial NCT02036632?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 12 participants. The study started on 2012-11. Estimated completion is 2015-01.
What interventions are being tested in trial NCT02036632?
The interventions under investigation include: Eye Patching (DEVICE).
Who is sponsoring clinical trial NCT02036632?
This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT02036632's enrollment target sits among peer trials
12 1852nd of 2000 higher than 90 of 2,000 other Phase 1 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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