Ripcord Removal for Glaucoma
What You Need to Know Before You Apply
What is the purpose of this trial?
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.
Who Is on the Research Team?
Leon W Herndon, MD
Principal Investigator
Duke University Eye Center
Are You a Good Fit for This Trial?
This trial is for people with glaucoma who have already had a glaucoma drainage device placed in their eye. Participants should be able to attend regular follow-up visits and are considering or due for ripcord removal as part of their care.Inclusion Criteria
Exclusion Criteria
What Are the Treatments Tested in This Trial?
Interventions
- Ripcord removal
Trial Overview
The study tests whether removing the ripcord from a glaucoma drainage device more than 3 months after surgery affects eye pressure. Eye pressure will be checked before and at several times after the ripcord is removed during routine clinic visits.
How Is the Trial Designed?
1
Treatment groups
Experimental Treatment
Find a Clinic Near You
Who Is Running the Clinical Trial?
Duke University
Lead Sponsor
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