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NCT01301378 · ClinicalTrials.gov registry record · NA
Patch Graft Material Safety and Effectiveness in Covering Glaucoma Drainage Device Tube
A NA study, sponsored by Wills Eye.
- Terminated
- Registry status
- NA
- Development phase
- 40
- Enrollment target
NCT01301378: Clinical Trial NA study, sponsored by Wills Eye.
NCT01301378 is a NA study that was terminated before completion, run by Wills Eye. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT01301378, a NA study, was terminated before completion, sponsored by Wills Eye.
- TERMINATED
- Registry status
- NA
- Development phase
- 40 participants
- Enrollment target
Study Summary
The investigators hypothesize that KeraSys is a safe as Tutoplast to cover the tube of the Molteno 3 glaucoma drainage device during surgery
Primary Outcome
The patch graft will be graded on appearance at each visit by slit lamp for tube erosion and conjunctival retraction.
Interventions
- PROCEDURE Molteno 3 glaucoma drainage shunt
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 40 participants |
| Start Date | 2010-08 |
| Est. Completion | 2011-01 |
| Phase | NA |
Why NCT01301378 stopped before completion
NCT01301378 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 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).
The record links to 0 conditions, and to 1 intervention - of which Molteno 3 glaucoma drainage shunt is the first listed.
NCT01301378 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT01301378 about?
NCT01301378 is a clinical study titled "Patch Graft Material Safety and Effectiveness in Covering Glaucoma Drainage Device Tube". The investigators hypothesize that KeraSys is a safe as Tutoplast to cover the tube of the Molteno 3 glaucoma drainage device during surgery
What is the current status of trial NCT01301378?
This trial is currently terminated. It is a NA study. The enrollment target is 40 participants. The study started on 2010-08. Estimated completion is 2011-01.
What interventions are being tested in trial NCT01301378?
The interventions under investigation include: Molteno 3 glaucoma drainage shunt (PROCEDURE).
Who is sponsoring clinical trial NCT01301378?
This trial is sponsored by Wills Eye, which has 59 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT01301378's enrollment target sits among peer trials
40 1447th of 2000 higher than 465 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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