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Evaluating the Efficacy of Fenestrations in Tube Shunt Implants During the Early Postoperative Period

Glaucoma Clinical Trial

Official title:
Evaluating the Efficacy of Fenestrations in Tube Shunt Implants During the Early Postoperative Period

Clinical Trial 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.

Clinical Trial Description

This is a prospective, randomized control study of glaucomatous eye undergoing tube shunt implantation using a nonvalved implant for poorly controlled glaucoma of any type. Eyes scheduled to receive a nonvalved tube shunt implant will be randomized to receive either needle fenestration(s) or a suture wick using a single 10-0 vicryl anterior to the ligature. The operative quadrant will be imaged using anterior-segment optical coherence tomography at pre- and post-operative visits. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02681419
Study type Interventional
Source The University of Texas Health Science Center, Houston
Contact
Status Terminated
Phase Phase 4
Start date January 2013
Completion date March 17, 2017
View Details
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