Viewing Study NCT00230763



Ignite Creation Date: 2024-05-05 @ 12:03 PM
Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00230763
Status: COMPLETED
Last Update Posted: 2021-02-18
First Post: 2005-09-29

Brief Title: Determination Of Predictive Factors Allowing To An Additional 10 Reduction Of Intra-Ocular Pressure
Sponsor: Pfizers Upjohn has merged with Mylan to form Viatris Inc
Organization: Pfizer

Study Overview

Official Title: Determination Of Predictive Factors Allowing To An Additional 10 Reduction Of Intra-Ocular Pressure After A 12-Week Treatment With Latanoprost 0005 Timolol 05 Fixed Combination Xalacom In Previously Treated Patients With Open Angle Glaucoma Or Ocular Hypertension
Status: COMPLETED
Status Verified Date: 2015-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: PREDICOM
Brief Summary: To determine the predictive factors of a positive response to latanoprost 0005 timolol 05 fixed combination defined as a 10 IOP reduction from baseline after 12 weeks of treatment age sex ethnic origin patients medical history family history of OAG or OHT concomitant systemic treatment with beta-blockers etiology IOP at baseline corneal thickness compliance and adverse events
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None