ICTRP Search Portal

Main

Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.

Register:	ClinicalTrials.gov
Last refreshed on:	19 October 2017
Main ID:	NCT01156012
Date of registration:	30/06/2010
Prospective Registration:	No
Primary sponsor:	Laboratoires Thea
Public title:	Efficacy and Safety Assessment of T2345 in Ocular Hypertensive or Glaucomatous Patients
Scientific title:
Date of first enrolment:	September 2009
Target sample size:	404
Recruitment status:	Completed
URL:	https://clinicaltrials.gov/show/NCT01156012
Study type:	Interventional
Study design:
Phase:	Phase 3

Countries of recruitment
France

Contacts

Key inclusion & exclusion criteria

Inclusion Criteria:

- Adult patients diagnosed with glaucoma

Exclusion Criteria:

- Under 18.

Age minimum: 18 Years
Age maximum: 90 Years
Gender: All

Health Condition(s) or Problem(s) studied

Glaucoma

Intervention(s)

Drug: T2345

Drug: Prostaglandin

Primary Outcome(s)

Change From Baseline in Intraocular Pressure (IOP) [Time Frame: Day 0 and Day 84]

Secondary Outcome(s)

Secondary ID(s)

LT2345-PIII-12/08

2009-011157-41

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Ethics review

Results

Results available:	Yes
Date Posted:	19/11/2014
Date Completed:
URL:	https://clinicaltrials.gov/ct2/show/results/NCT01156012

Disclaimer: Trials posted on this search portal are not endorsed by WHO, but are provided as a service to our users. In no event shall the World Health Organization be liable for any damages arising from the use of the information linked to in this section. None of the information obtained through use of the search portal should in any way be used in clinical care without consulting a physician or licensed health professional. WHO is not responsible for the accuracy, completeness and/or use made of the content displayed for any trial record.