Lipid Profile of Tenon's Capsule
This study has been completed.
Sponsor:
Centre Hospitalier Universitaire Dijon
Information provided by:
Centre Hospitalier Universitaire Dijon
ClinicalTrials.gov Identifier:
NCT01021657
First received: November 27, 2009
Last updated: NA
Last verified: November 2009
History: No changes posted
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Purpose
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.
| Condition | Intervention |
|---|---|
|
Glaucoma |
Procedure: trabeculectomies, non penetrating deep sclerectomies |
| Study Type: | Observational |
| Study Design: | Observational Model: Cohort Time Perspective: Prospective |
| Official Title: | Lipid Profile of Tenon's Capsule in Glaucoma Patients |
Resource links provided by NLM:
Genetics Home Reference related topics:
early-onset glaucoma
MedlinePlus related topics:
Glaucoma
U.S. FDA Resources
Further study details as provided by Centre Hospitalier Universitaire Dijon:
Primary Outcome Measures:
- 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. [ Time Frame: 6 month later ] [ Designated as safety issue: No ]
Biospecimen Retention: Samples Without DNA
Eye Tenon's Capsule
| Enrollment: | 27 |
| Study Start Date: | January 2009 |
| Study Completion Date: | June 2009 |
| Primary Completion Date: | June 2009 (Final data collection date for primary outcome measure) |
| Groups/Cohorts | Assigned Interventions |
|---|---|
| Glaucoma | Procedure: trabeculectomies, non penetrating deep sclerectomies |
Eligibility| Ages Eligible for Study: | 18 Years to 90 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
| Sampling Method: | Non-Probability Sample |
Study Population
Patient suffering from Glaucoma
Criteria
Inclusion Criteria:
- Glaucoma
- Eligibility for surgery
Exclusion Criteria:
- Patients without Glaucoma
Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT01021657
Locations
| France | |
| Ophthalmology Unit CHU Dijon | |
| Dijon, France, 21000 | |
Sponsors and Collaborators
Centre Hospitalier Universitaire Dijon
Investigators
| Principal Investigator: | Catherine Creuzot-Gracher, MD, PhD | Ophthalmology unit CHU Dijon |
More Information
No publications provided
| Responsible Party: | Professor Catherine Creuzot-Garcher, Ophthalmology Department |
| ClinicalTrials.gov Identifier: | NCT01021657 History of Changes |
| Other Study ID Numbers: | Alain01 |
| Study First Received: | November 27, 2009 |
| Last Updated: | November 27, 2009 |
| Health Authority: | France: Afssaps - Agence française de sécurité sanitaire des produits de santé (Saint-Denis) |
Keywords provided by Centre Hospitalier Universitaire Dijon:
|
Glaucoma Tenon's Capsule Lipid profile Assessment of lipid profile in Tenon's capsule in patients with Glaucoma |
Additional relevant MeSH terms:
|
Glaucoma Ocular Hypertension Eye Diseases |
ClinicalTrials.gov processed this record on May 16, 2013