Anatomical and Functional Macular Changes in Retinal Detachment

This study has been completed.
Sponsor:
Information provided by:
Centre Hospitalier Universitaire Dijon
ClinicalTrials.gov Identifier:
NCT01343134
First received: April 26, 2011
Last updated: May 12, 2011
Last verified: January 2011
  Purpose

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.


Condition Intervention
Rhegmatogenous Retinal Detachment
Device: Measure the outer retina by spectral domain optical coherence tomography (HRA Spectralis; Heidelberg), and microperimetry (OPKO Instruments)

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Retrospective

Resource links provided by NLM:


Further study details as provided by Centre Hospitalier Universitaire Dijon:

Enrollment: 30
Study Start Date: January 2010
Study Completion Date: December 2010
Primary Completion Date: June 2010 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Retinal detachment cohort 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.

  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

Patients with successful repair of rhegmatogenous retinal detachment after macula off and minimum 6 month follow-up after surgery

Criteria

Inclusion Criteria:

  • Rhegmatogenous retinal detachment

Exclusion Criteria:

  • Epiretinal membrane
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01343134

Locations
France
Ophthalmology Department CHU Dijon
Dijon, Burgundy, France, 21000
Sponsors and Collaborators
Centre Hospitalier Universitaire Dijon
Investigators
Study Director: Catherine Creuzot-Garcher, MD;PhD Ophthalmology department CHU Dijon
Principal Investigator: Marie Pierre Delolme, MD Ophthalmology Department CHU Dijon
  More Information

No publications provided

Responsible Party: Pr Catherine Creuzot-Garcher, Ophthalmology department
ClinicalTrials.gov Identifier: NCT01343134     History of Changes
Other Study ID Numbers: Marie Pierre 01
Study First Received: April 26, 2011
Last Updated: May 12, 2011
Health Authority: France: Direction Générale de la Santé

Keywords provided by Centre Hospitalier Universitaire Dijon:
Retina
Rhegmatogenous retinal detachment
Macular detachment
Spectral domain OCT
Microperimetry

Additional relevant MeSH terms:
Retinal Detachment
Dissociative Disorders
Retinal Diseases
Eye Diseases
Mental Disorders

ClinicalTrials.gov processed this record on August 18, 2014