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:	NCT01155999
Date of registration:	30/06/2010
Prospective Registration:	No
Primary sponsor:	Laboratoires Thea
Public title:	Clinical Efficacy and Safety of T1225 Versus Tobramycin 0.3 % Eye Drops in the Treatment of Purulent Bacterial Conjunctivitis of Children.
Scientific title:
Date of first enrolment:	December 2008
Target sample size:	286
Recruitment status:	Completed
URL:	https://clinicaltrials.gov/show/NCT01155999
Study type:	Interventional
Study design:
Phase:	Phase 3

Countries of recruitment
France

Contacts

Key inclusion & exclusion criteria

Inclusion Criteria:

- Age = one day of life and = 18 years

- Purulent bacterial conjunctivitis

Age minimum: N/A
Age maximum: 18 Years
Gender: All

Health Condition(s) or Problem(s) studied

Purulent Bacterial Conjunctivitis

Intervention(s)

Drug: Tobramycin

Drug: T1225

Primary Outcome(s)

The Primary Efficacy Variable Was Clinical Cure in the Worse Eye on Day 3 [Time Frame: Day 3]

Secondary Outcome(s)

Secondary ID(s)

LT1225-PIIIB-02/08

2008-003567-39

Source(s) of Monetary Support

Please refer to primary and secondary sponsors

Secondary Sponsor(s)

Ethics review

Results

Results available:	Yes
Date Posted:	29/10/2014
Date Completed:
URL:	https://clinicaltrials.gov/ct2/show/results/NCT01155999

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.