Geneva, April 27 -- International Clinical Trials Registry received information related to the study (NCT07531199) titled 'Efficacy and Safety of a Releasable Intraluminal Suture Technique to Reduce Hypotony Following Glaucoma Surgery Using the Preserflo Device' on April 9.
Study Type: Interventional
Study Design:
Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Participant, Outcomes Assessor).
Primary Sponsor: Hopital Prive de la Baie
Condition:
Glaucoma
Intervention:
Procedure: Classical surgery
Recruitment Status: Not recruiting
Phase: N/A
Date of First Enrollment: May 1, 2026
Target Sample Size: 192
To know more, visit https://clinicaltrials.gov/study/NCT075...