24-hour Intraocular Pressure (IOP) Control With the Bimatoprost/Timolol Fixed Combination (BTFC)

This study has been completed.

Sponsor:

Information provided by (Responsible Party):

AGP Konstas, Aristotle University Of Thessaloniki

ClinicalTrials.gov Identifier:

NCT00486486

First received: June 13, 2007

Last updated: January 25, 2013

Last verified: January 2013

History of Changes

No Study Results Posted on ClinicalTrials.gov for this Study

About Study Results Reporting on ClinicalTrials.gov

Study Status:	This study has been completed.
Study Completion Date:	July 2008
Primary Completion Date:	May 2008 (Final data collection date for primary outcome measure)

No publications provided by Aristotle University Of Thessaloniki

Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):

Konstas AG, Holló G, Mikropoulos D, Tsironi S, Haidich AB, Embeslidis T, Georgiadou I, Irkec M, Melamed S. Twenty-four-hour intraocular pressure control with bimatoprost and the bimatoprost/timolol fixed combination administered in the morning, or evening in exfoliative glaucoma. Br J Ophthalmol. 2010 Feb;94(2):209-13. Epub 2009 Oct 12.

To Top