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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01343134
Other study ID # Marie Pierre 01
Secondary ID
Status Completed
Phase N/A
First received April 26, 2011
Last updated May 12, 2011
Start date January 2010
Est. completion date December 2010

Study information

Verified date January 2011
Source Centre Hospitalier Universitaire Dijon
Contact n/a
Is FDA regulated No
Health authority France: Direction Générale de la Santé
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate the correlation between morphologic changes in the outer retina and visual function after successful repair of rhegmatogenous retinal detachment with macula off.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date December 2010
Est. primary completion date June 2010
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 90 Years
Eligibility Inclusion Criteria:

- Rhegmatogenous retinal detachment

Exclusion Criteria:

- Epiretinal membrane

Study Design

Observational Model: Cohort, Time Perspective: Retrospective


Related Conditions & MeSH terms


Intervention

Device:
Measure the outer retina by spectral domain optical coherence tomography (HRA Spectralis; Heidelberg), and microperimetry (OPKO Instruments)
Measure the thickness of the outer retina by spectral domain optical coherence tomography (HRA Spectralis; Heidelberg)and perform central microperimetry using new OPKO Instruments OCT.

Locations

Country Name City State
France Ophthalmology Department CHU Dijon Dijon Burgundy

Sponsors (1)

Lead Sponsor Collaborator
Centre Hospitalier Universitaire Dijon

Country where clinical trial is conducted

France, 

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