CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 37 enrolled
Drug / intervention
Latanoprost, Dorzolamidedrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01527682
NCT01527682Phase 2Completed

Efficacy and Safety of Prostaglandin Analogue and Carbonic Anhydrase Inhibitor for the Treatment of Pediatric Glaucoma

Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia·interventional·Posted Feb 7, 2012·Updated Sep 27, 2019

In Brief

A Phase 2 clinical trial evaluating Latanoprost, Dorzolamide for Childhood Glaucoma. Completed, enrolled 37 participants across 2 sites.

Detailed Summary

Objectives: The study will assess the ocular hypotensive effect of latanoprost and dorzolamide in a selected sample of patients affected by primary Pediatric Glaucoma (PG), refractory to surgical procedures. Safety will be assessed, too.In the first version of the protocol 96 eyes were forecasted to complete the enrolment. The protocol was then amended and now to complete the study 68 eyes should be included. This number of eyes could be achieved by recruiting from 34 to 68 patients due to not in all patients both eyes should be eligible for the study.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesItaly
Collaborators--

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedFeb 7, 2012
Enrollment StartJul 1, 2009
Primary CompletionNov 1, 2016
TodayJul 2, 2026
Enrollment to primary: 7.3 yearsPosted 14.4 years ago

Interventions

Latanoprost, Dorzolamidedrug

* Latanoprost 0.005% ophthalmic solution given once a day at nighttime (9.00 PM) * Dorzolamide 2% ophthalmic solution given three times a day as a monotherapy, two times a day if in combination with latanoprost