Corneal Versus Conjunctival Delivery Using a Delivery Device
This study has been withdrawn prior to enrollment.
Sponsor:
Pfizer
Information provided by:
Pfizer
ClinicalTrials.gov Identifier:
NCT00143429
First received: September 1, 2005
Last updated: March 1, 2007
Last verified: October 2006
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Purpose
Compare the antihypertensive efficacy of three methods for installing Xalatan
| Condition | Intervention | Phase |
|---|---|---|
|
Glaucoma, Open-Angle Ocular Hypertension |
Drug: Xalatan |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Crossover Assignment Masking: Single Blind Primary Purpose: Treatment |
| Official Title: | Effect Of Corneal Versus Conjunctival Delivery On The Corneal Safety, Tolerability, and Antihypertensive Efficacy Of The Xalatan Ophthalmic Delivery Device |
Resource links provided by NLM:
Genetics Home Reference related topics:
early-onset glaucoma
Drug Information available for:
Latanoprost
U.S. FDA Resources
Further study details as provided by Pfizer:
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Criteria
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
Contacts and Locations
More Information
No publications provided
| ClinicalTrials.gov Identifier: | NCT00143429 History of Changes |
| Other Study ID Numbers: | A6111127 |
| Study First Received: | September 1, 2005 |
| Last Updated: | March 1, 2007 |
| Health Authority: | United States: Food and Drug Administration |
Keywords provided by Pfizer:
|
Primary Open Angle Glaucoma |
Additional relevant MeSH terms:
|
Glaucoma Glaucoma, Open-Angle Hypertension Ocular Hypertension Eye Diseases Vascular Diseases |
Cardiovascular Diseases Latanoprost Antihypertensive Agents Cardiovascular Agents Therapeutic Uses Pharmacologic Actions |
ClinicalTrials.gov processed this record on May 22, 2013