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Randomized,Active Comparator-Controlled,Three Months,Open Label Clinical Trial to Compare Efficacy and Safety of Refrigeration-Free Latanoprost (0.005%) and Latanoprost (0.005%) Stored at Refrigeration Temperature in Patients With OAG or OHT
The purpose of this study is to: * To evaluate the efficacy of Refrigeration-Free Latanoprost compared to Latanoprost stored at refrigeration temperature with respect to the diurnal intraocular pressure (IOP) change from baseline after 3 months of therapy in patients with open-angle glaucoma (OAG) or ocular hypertension. * To evaluate the safety and tolerability of Refrigeration-Free Latanoprost in patients with open-angle glaucoma (OAG) or ocular hypertension.
Details
| Lead sponsor | Aurolab |
|---|---|
| Phase | NA |
| Status | UNKNOWN |
| Enrolment | 30 |
| Start date | 2011-09 |
| Completion | 2012-08 |
Conditions
- Glaucoma, Open-Angle
- Ocular Hypertension
Interventions
- refrigeration free latanoprost
- latanoprost eye drops
Primary outcomes
- Intraocular pressure — 3 months
to evalate the change in intraocular pressure from baseline to end of treatment
Countries
India