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Completed NCT07592923

Morphometric Markers of the Effectiveness of Micropulse Cyclophotocoagulation

Conditions: Glaucoma

Sex: All
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 20
Sponsor: Kazakh Eye Research Institute

Location: Kazakh Eye Research Institute Almaty

Summary

This prospective study aims to evaluate morphometric markers of treatment response following micropulse transscleral cyclophotocoagulation (MP-CPC) in patients with glaucoma. The study will assess changes in choroidal thickness and the choroidal vascularity index (CVI) measured by optical coherence tomography (OCT) before treatment, 3-7 days after the procedure, and 1 month postoperatively. Intraocular pressure (IOP) will be measured at the same time points. The correlation between changes in choroidal thickness, the choroidal vascularity index (CVI) and IOP reduction will be analyzed. Additionally, the study seeks to determine the minimal baseline choroidal thickness associated with a clinically significant hypotensive effect after MP-CPC.

Eligibility Criteria

Inclusion Criteria: * Decision to treat by MP-CPC Laser * Patients diagnosed with Glaucoma * Patients aged 18 years old and above * Glaucoma that is inadequately controlled on medical therapy Exclusion Criteria: * Patients age less than 18 years * Patients unable or unwilling to provide informed consent to participate in the study * Patients potentially unavailable for follow up visits * Patients with significant scleral thinning * Patients with ocular infection, inflammation or intraocular surgery in the study eye 2 months prior to enrollment in the study * Albino patients that have no iris pigmentation

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View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07592923). StuddyBuddy aggregates publicly available trial information.