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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01021657
Other study ID # Alain01
Secondary ID
Status Completed
Phase N/A
First received November 27, 2009
Last updated November 27, 2009
Start date January 2009
Est. completion date June 2009

Study information

Verified date November 2009
Source Centre Hospitalier Universitaire Dijon
Contact n/a
Is FDA regulated No
Health authority France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis)
Study type Observational

Clinical Trial Summary

The purpose of this study is to provide data on the lipid profile of the Tenon's capsule in Human glaucomatous eyes and to establish possible relationships with the short term outcome of filtration surgery.


Recruitment information / eligibility

Status Completed
Enrollment 27
Est. completion date June 2009
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Glaucoma

- Eligibility for surgery

Exclusion Criteria:

- Patients without Glaucoma

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Procedure:
trabeculectomies, non penetrating deep sclerectomies


Locations

Country Name City State
France Ophthalmology Unit CHU Dijon Dijon

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary To provide data on the lipid profile of the Tenon's capsule in Human glaucomatous eyes and to establish possible relationships with the short term outcome of filtration surgery. 6 month later No
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