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Clinical Trials/JPRN-UMIN000034108
JPRN-UMIN000034108Completed未知

The efficacy and safety of Latanoprost ophthalmic solution 0.005% Nitten in Japanese open-angle glaucoma patients - The efficacy and safety of Latanoprost ophthalmic solution 0.005% Nitten in Japanese open-angle glaucoma patients

The University of Tokyo Hospital0 sites0 target enrollmentStarted: September 17, 2018Last updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed

Study Overview

Brief Summary

ot applicable

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
20years-old to 80years-old (—)
Sex
All

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • 1. With a history of eye surgery including laser 2. Having allergy to prostaglandin related drug 3. Using ophthalmic or internal steroids 4. Oral administration of acetazolamide (Diamox) 5. The contact lenses are scheduled to be used during the test period 6. Persons who judged that the doctor in charge is not appropriate

Investigators

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