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Comparison of Phaco Surgery With Goniosynechialysis Versus Trabeculectomy in Glaucoma Treatment

StatusRecruiting
PhaseNot applicable
Started
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Record History

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  1. Study description revisedv8
  2. Primary endpoints: 2 to 1
    • Enrollment target: 80 to 82
    • Primary completion date: Jul 10, 2027 to Jul 30, 2027
    • Secondary endpoints: 3 to 4
    v7
  3. Trial status: Not Yet Recruiting to Recruiting
    • Site details revised
    v6
  4. Re-verified, no change to tracked fieldsv5
  5. Start date: Apr 10, 2025 to Jun 1, 2025v4 Show 4 more changesShow less
    • Trial status: Enrolling by Invitation to Not Yet Recruiting
    • Primary completion date: Apr 10, 2027 to Jul 10, 2027
    • Study completion date: Jun 10, 2027 to Sep 10, 2027
    • Eligibility criteria expanded, about 35 words
Show 2 earlier versionsHide 2 earlier versions
  1. Study description revisedv3
  2. Eligibility criteria expanded, about 8 wordsv2
  1. Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The goal of this clinical trial is to learn whether phacoemulsification combined with goniosynechialysis (Phaco-GSL) is as effective and safe as trabeculectomy in treating patients with primary angle-closure glaucoma. The main questions it aims to answer are: * Does Phaco-GSL provide similar or better intraocular pressure (IOP) control compared to trabeculectomy? * What are the rates of postoperative complications or adverse events between the two surgical approaches? * How do the two procedures compare in terms of visual acuity recovery and need for glaucoma medications? Researchers will compare Phaco-GSL to trabeculectomy to determine which procedure offers better overall outcomes for patients with angle-closure glaucoma. Participants will: Be randomly assigned to undergo either Phaco-GSL or trabeculectomy Attend scheduled follow-up visits at regular intervals (e.g., 1 week, 1 month, 3 months, 6 months, 12 months) for eye exams and pressure checks
Trial Details
NCT Number NCT06952153
Lead Sponsor University of Medicine and Pharmacy at Ho Chi Minh City
Conditions
(from sponsor)		 Primary Angle Closure Glaucoma
Related terms Glaucoma, Angle-Closure
Enrollment 82 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov