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NCT01020656 Clinical Trial

Anticoagulant and Antiplatelet Agents in Patients Undergoing Vitreoretinal Surgery

Retinal Detachment Clinical Trial

Official title:
Maintenance of Anticoagulant and Antiplatelet Agents for Patients Undergoing Vitreoretinal Surgery

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT01020656
Other study ID # MARIE02
Secondary ID
Status Completed
Phase N/A
First received November 24, 2009
Last updated November 24, 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

Purpose: To establish the prevalence of anticoagulant, aspirin, and clopidogrel use in patients undergoing vitreoretinal surgery, and to compare the outcome of peribulbar anesthesia between users and non-users.

Recruitment information / eligibility
Status Completed
Enrollment 206
Est. completion date June 2009
Est. primary completion date June 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Take or no anticoagulant treatment before surgery,

- Vitreoretinal surgery

Exclusion Criteria:none

- No surgery

- Anesthetic complication

Study Design

Observational Model: Cohort, Time Perspective: Retrospective

Related Conditions & MeSH terms

Locations
Country Name City State
France Ophthalmology Unit CHU Dijon Dijon Burgundy

Sponsors (1)
Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

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