Prospective Study of the Diagnostic and Therapeutic Management of Congenital Glaucoma in France (Conglau)
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|ClinicalTrials.gov Identifier: NCT03077789|
Recruitment Status : Recruiting
First Posted : March 13, 2017
Last Update Posted : October 16, 2019
Evidence of a relationship between age at discovery of congenital glaucoma and visual acuity at 4 years of age.
The delay in diagnosis is a factor of poor visual acuity. Will justify the implementation of information programs with health and education professionals in order to improve the functional prognosis of patients with congenital glaucoma.
|Condition or disease||Intervention/treatment||Phase|
|Congenital Glaucoma||Procedure: TRABECULOTOMY||Not Applicable|
Prospective multicentre prospective cohort Enabling the identification and follow-up of an almost exhaustive population of incidents of congenital glaucoma in 23 ophthalmology centers in France Inclusion over 4 years Epidemiological data, all reports of consultation, medical and surgical procedures collected in an E-CRF.
Database for gene research related to congenital glaucoma to provide screening, genetic counseling and personalized care
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||250 participants|
|Intervention Model:||Single Group Assignment|
|Masking:||None (Open Label)|
|Official Title:||Prospective Study of the Diagnostic and Therapeutic Management of Congenital Glaucoma in France|
|Actual Study Start Date :||April 2013|
|Estimated Primary Completion Date :||April 2023|
|Estimated Study Completion Date :||April 2023|
Evaluation of the prognosis of different surgery in congenital glaucoma
Other Name: sclerectomy needling trabeculectomy
- Visual acuity by logarithmic scale of Sander-Zanlonghi [ Time Frame: at 4 years of the child ]Evidence of a relationship between age at discovery of congenital glaucoma and visual acuity at 4 years of age
- Intraocular pressure [ Time Frame: at 4 years of the child ]measure intraocular pressure (Tonopen or Perkins initially, air tonometer or Goldman as soon as possible) for prognosis of congenital glaucoma
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT03077789
|Contact: Jean-François ROULAND, MD,PhDfirstname.lastname@example.org|
|CHRU, Hôpital Claude Huriez||Recruiting|
|Principal Investigator: Jean-François ROULAND, MD,PhD|
|Principal Investigator:||Jean-François ROULAND, MD, PhD||University Hospital, Lille|