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NCT02681419 · ClinicalTrials.gov registry record · Phase 4
Evaluating the Efficacy of Fenestrations in Tube Shunt Implants During the Early Postoperative Period
A Phase 4 study, sponsored by The University of Texas Health Science Center, Houston.
- Terminated
- Registry status
- Phase 4
- Development phase
- 18
- Enrollment target
NCT02681419 is a Phase 4 study that was terminated before completion, run by The University of Texas Health Science Center, Houston. The registered enrollment target is 18 participants.
The verdict
NCT02681419, a Phase 4 study, was terminated before completion, sponsored by The University of Texas Health Science Center, Houston.
- TERMINATED
- Registry status
- Phase 4
- Development phase
- 18 participants
- Enrollment target
Study Summary
This study evaluates two different methods of controlling intraocular pressure in nonvalved aqueous tube shunts immediately after implantation; needle fenestrations or a suture wick.
Interventions
- PROCEDURE Needle fenestration
- PROCEDURE Suture wick
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 18 participants |
| Start Date | 2013-01 |
| Est. Completion | 2017-03-17 |
| Phase | Phase 4 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT02681419
The ClinicalTrials.gov registry entry for NCT02681419 describes a study currently listed as terminated, categorized as Phase 4. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The University of Texas Health Science Center, Houston, which has 732 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Needle fenestration is the first listed.
NCT02681419 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT02681419 about?
NCT02681419 is a clinical study titled "Evaluating the Efficacy of Fenestrations in Tube Shunt Implants During the Early Postoperative Period". This study evaluates two different methods of controlling intraocular pressure in nonvalved aqueous tube shunts immediately after implantation; needle fenestrations or a suture wick.
What is the current status of trial NCT02681419?
This trial is currently terminated. It is a Phase 4 study. The enrollment target is 18 participants. The study started on 2013-01. Estimated completion is 2017-03-17.
What interventions are being tested in trial NCT02681419?
The interventions under investigation include: Needle fenestration (PROCEDURE), Suture wick (PROCEDURE).
Who is sponsoring clinical trial NCT02681419?
This trial is sponsored by The University of Texas Health Science Center, Houston, which has 732 total clinical trials registered on ClinicalTrials.gov.
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