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NCT00143429 Clinical Trial

Corneal Versus Conjunctival Delivery Using a Delivery Device

Ocular Hypertension Clinical Trial

Official title:
Effect Of Corneal Versus Conjunctival Delivery On The Corneal Safety, Tolerability, and Antihypertensive Efficacy Of The Xalatan Ophthalmic Delivery Device

Clinical Trial Details — Status: Withdrawn

Administrative data
NCT number NCT00143429
Other study ID # A6111127
Secondary ID
Status Withdrawn
Phase Phase 2
First received
Last updated

Study information
Verified date March 2015
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Compare the antihypertensive efficacy of three methods for installing Xalatan

Recruitment information / eligibility
Status Withdrawn
Enrollment 0
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Diagnosis of primary open angle glaucoma or ocular hypertension in 1 or both eyes Exclusion Criteria: - History of closed/barely open anterior chamber angle or a history of angle closure

Study Design

Related Conditions & MeSH terms

Intervention

Drug:
• Xalatan

Locations
Country Name City State
n/a

Sponsors (1)
Lead Sponsor Collaborator
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.

Outcome
Type Measure Description Time frame Safety issue
Primary IOP level in the study eye
Secondary Change in ocular safety assessments. Ocular and systemic adverse events throughout the study period
See also
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