Trial ID or NCT#

NCT04285580

Status

not recruiting iconNOT RECRUITING

Purpose

This study will evaluate the 24-hour intraocular pressure lowering effect and safety after a single administration of Bimatoprost SR in patients with Open-Angle Glaucoma or Ocular Hypertension

Official Title

An Evaluation of the 24-Hour Intraocular Pressure(IOP)-Lowering Effect of Bimatoprost Sustained-Release(SR) in Participants With Open-Angle Glaucoma(OAG) or Ocular Hypertension(OHT)

Eligibility Criteria

Ages Eligible for Study: Older than 18 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No

Investigator(s)

Ann Caroline Fisher, MD
Ann Caroline Fisher, MD
Glaucoma specialist, Cataract specialist
Clinical Associate Professor, Ophthalmology

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CONTACT

SPECTRUM