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NCT00818844 · ClinicalTrials.gov registry record · Phase 4
Role of Nepafenac in Reducing Macular Volume After Epiretinal Membrane Surgery
A Phase 4 study, sponsored by Alcon Research.
- Completed
- Registry status
- Phase 4
- Development phase
- 40
- Enrollment target
NCT00818844: Completed Phase 4 study, sponsored by Alcon Research.
NCT00818844 is a Phase 4 study that has completed, run by Alcon Research. The registered enrollment target is 40 participants, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT00818844, a Phase 4 study, has completed, sponsored by Alcon Research.
- COMPLETED
- Registry status
- Phase 4
- Development phase
- 40 participants
- Enrollment target
Study Summary
The purpose of this study is to compare the macular volume of patients treated with a 3-month course of topical Nepafenac (0.1% solution) to patients treated with a placebo course following epiretinal membrane surgery.
Primary Outcome
Macular thickness as measured by SD-OCT
Interventions
- DRUG Nepafenac 0.1%
- OTHER BSS
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2009-01 |
| Est. Completion | 2010-06 |
| Phase | Phase 4 |
What the finished NCT00818844 record still lists
NCT00818844 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 518-participant average among 9,235 other Phase 4 trials with a reported enrollment target (92% lower).
The record links to 0 conditions, and to 2 interventions - of which Nepafenac 0.1% is the first listed.
NCT00818844 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT00818844 about?
NCT00818844 is a clinical study titled "Role of Nepafenac in Reducing Macular Volume After Epiretinal Membrane Surgery". The purpose of this study is to compare the macular volume of patients treated with a 3-month course of topical Nepafenac (0.1% solution) to patients treated with a placebo course following epiretinal membrane surgery.
What is the current status of trial NCT00818844?
This trial is currently completed. It is a Phase 4 study. The enrollment target is 40 participants. The study started on 2009-01. Estimated completion is 2010-06.
What interventions are being tested in trial NCT00818844?
The interventions under investigation include: Nepafenac 0.1% (DRUG), BSS (OTHER).
Who is sponsoring clinical trial NCT00818844?
This trial is sponsored by Alcon Research, which has 275 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT00818844's enrollment target sits among peer trials
40 1397th of 2000 higher than 533 of 2,000 other Phase 4 trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Phase 4 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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