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...