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NCT05615805 · ClinicalTrials.gov registry record · NA
The Effect of Ocular Rinse Volume on Surface Irritation After Intravitreal Injections
A NA study, sponsored by University of Oklahoma.
- Completed
- Registry status
- NA
- Development phase
- 142
- Enrollment target
NCT05615805: Completed NA study, sponsored by University of Oklahoma.
NCT05615805 is a NA study that has completed, run by University of Oklahoma. The registered enrollment target is 142 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05615805, a NA study, has completed, sponsored by University of Oklahoma.
- COMPLETED
- Registry status
- NA
- Development phase
- 142 participants
- Enrollment target
Study Summary
This is the first randomized controlled trial looking into post-injection rinse volume of standard ophthalmic eyewash and its affect on patient comfort up to 72 hours after injections.
Primary Outcome
Patient symptoms questionnaire, range 0-28, higher score is associated with worse outcome.
Interventions
- OTHER OSDI questionnaire
- OTHER SPEEDII questionnaire
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 142 participants |
| Start Date | 2021-03-01 |
| Est. Completion | 2021-10-01 |
| Phase | NA |
What the finished NCT05615805 record still lists
NCT05615805 is an interventional study that assigns participants to a tested intervention. The registered 142 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).
The record links to 0 conditions, and to 2 interventions - of which OSDI questionnaire is the first listed.
NCT05615805 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05615805 about?
NCT05615805 is a clinical study titled "The Effect of Ocular Rinse Volume on Surface Irritation After Intravitreal Injections". This is the first randomized controlled trial looking into post-injection rinse volume of standard ophthalmic eyewash and its affect on patient comfort up to 72 hours after injections.
What is the current status of trial NCT05615805?
This trial is currently completed. It is a NA study. The enrollment target is 142 participants. The study started on 2021-03-01. Estimated completion is 2021-10-01.
What interventions are being tested in trial NCT05615805?
The interventions under investigation include: OSDI questionnaire (OTHER), SPEEDII questionnaire (OTHER).
Who is sponsoring clinical trial NCT05615805?
This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05615805's enrollment target sits among peer trials
142 711th of 2000 higher than 1,289 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA 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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