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Clinical Trial Summary

The objectives of this study are: - To assess the effect of ophthalmic phentolamine mesylate in mesopic conditions on the four endpoints: 1. Contrast sensitivity 2. Low contrast visual acuity 3. Wavefront aberrometry 4. Subjective questionnaire - To assess the safety of ophthalmic phentolamine mesylate


Clinical Trial Description

Double-masked, placebo-controlled, single-dose Phase 2 study in 24 patients experiencing severe night vision difficulties to evaluate ocular and systemic safety and efficacy following administration of one drop of phentolamine mesylate 1.0% QD in each eye for 1 day. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04004507
Study type Interventional
Source Ocuphire Pharma, Inc.
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Status Completed
Phase Phase 2
Start date August 2007
Completion date February 2008

See also
  Status Clinical Trial Phase
Completed NCT01703559 - The Safety and Efficacy of Phentolamine Mesylate Ophthalmic Solution in Subjects With Severe Night Vision Disturbances Phase 2