drugset / Trial / NCT05606796

Comparison of Preserved and Preservative-free Latanoprost 0.005% in Primary Open Angle Glaucoma and Ocular Hypertensive Patients, at Guinness Eye Centre, Lagos.

NCT05606796

Phase 4 Unknown 76 enrolled Uzoma Chinyei Joan
RandomizedParallel-groupDouble-blindTreatment

Summary

It is a randomised, double-blinded clinical trial in which consenting participants who meet the inclusion criteria would be randomised into 2 groups. Subjects will be given either preserved or preservative free latanoprost for a period of 12 weeks. The efficacy and tolerability of both drugs would be assessed every 4 weeks, amongst these patients.

Timeline

Start
2022-12
Primary completion
2023-08
Completion
2023-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Latanoprost Small molecule 0.005 % Topical

Indications

No indication recorded.