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NCT01786954 · ClinicalTrials.gov registry record · NA
iCare vs Tonopen vs Goldmann Applanation Post-vitrectomy Surgery
A NA study, sponsored by Duke University.
- Completed
- Registry status
- NA
- Development phase
- 68
- Enrollment target
NCT01786954: Completed NA study, sponsored by Duke University.
NCT01786954 is a NA study that has completed, run by Duke University. The registered enrollment target is 68 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01786954, a NA study, has completed, sponsored by Duke University.
- COMPLETED
- Registry status
- NA
- Development phase
- 68 participants
- Enrollment target
Study Summary
The purpose of the study is to compare the measurement of pressure inside the eye using three different FDA-approved devices (Icare, Tonopen, and Goldmann applanation).
Primary Outcome
The primary outcome is the measurement of intraocular pressure on postoperative day #1 following vitreoretinal surgery.
Interventions
- DEVICE Icare rebound tonometry
- DEVICE Tonopen applanation
- DEVICE Goldmann applanation
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 68 participants |
| Start Date | 2012-10 |
| Est. Completion | 2014-09 |
| Phase | NA |
What the finished NCT01786954 record still lists
NCT01786954 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 68 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (95% lower).
The record links to 0 conditions, and to 3 interventions - of which Icare rebound tonometry is the first listed.
NCT01786954 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01786954 about?
NCT01786954 is a clinical study titled "iCare vs Tonopen vs Goldmann Applanation Post-vitrectomy Surgery". The purpose of the study is to compare the measurement of pressure inside the eye using three different FDA-approved devices (Icare, Tonopen, and Goldmann applanation).
What is the current status of trial NCT01786954?
This trial is currently completed. It is a NA study. The enrollment target is 68 participants. The study started on 2012-10. Estimated completion is 2014-09.
What interventions are being tested in trial NCT01786954?
The interventions under investigation include: Icare rebound tonometry (DEVICE), Tonopen applanation (DEVICE), Goldmann applanation (DEVICE).
Who is sponsoring clinical trial NCT01786954?
This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01786954's enrollment target sits among peer trials
68 1133rd of 2000 higher than 862 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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