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Effect of Late Ripcord Removal From Glaucoma Drainage Device

Name: Effect of Late Ripcord Removal From Glaucoma Drainage Device — clinical trial record (NCT07803536)
Creator: DataLookout
License: https://creativecommons.org/licenses/by/4.0/

StatusNot Yet Recruiting

PhaseNot applicable

SponsorDuke University

Started2026-09

View on ClinicalTrials.gov ↗

Duke University

455 trials monitored

See 53 trials at risk

This is a research study to find out if removing the ripcord from a glaucoma drainage device more than 3 months after it has been placed has any effect on intraocular pressure. Participation in research studies is voluntary. The ripcord will be removed at a routine glaucoma care visit and intraocular pressure will be measured before removal, 30 minutes following, and at 1 week, 6 weeks and 3-month intervals during regular clinic visits.

Trial Details

NCT Number	NCT07803536
Lead Sponsor	Duke University
Conditions	GLAUCOMA 1, OPEN ANGLE, D (Disorder), Glaucoma
Enrollment	80 participants
Start Date	2026-09
Primary Completion	2028-09 (estimated)
Study Completion	2028-12 (estimated)
Updated on ClinicalTrials.gov	2026-09-03