drugset / Trial / NCT01979913

An Open, Non-randomized Pilot Study on the Effect of Preservative Free Tafluprost (Saflutan® Augentropfen) in Patients With Ocular Hypertension or Primary Open Angle Glaucoma With an Uncontrolled Intraocular Pressure of 30 mmHg and More

NCT01979913

Phase 4 Completed 16 enrolled Dr. Anton Hommer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Increased intraocular pressure (IOP) has been identified as the most important risk factor for the development and the progression of glaucoma. Data from large interventional studies have shown that a decrease of IOP is associated with a reduced risk of progression of the disease. This underlines the importance of a potent and save IOP lowering therapy. The introduction of preservative free tafluprost offers a new treatment possibility using a potent topical prostaglandin analogue without the disadvantages of a co-administered preservative. The current study seeks to investigate the effect of an 8 week therapy with preservative free tafluprost on intraocular pressure in patients with ocular hypertension or primary open angle glaucoma having an IOP of 30 mmHg or more.

Timeline

Start
2013-10
Primary completion
2014-04
Completion
2014-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Tafluprost Other / unclassified 15 ug/ml Topical