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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04634786
Other study ID # 2020-A02305-34
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date February 6, 2021
Est. completion date August 6, 2021

Study information

Verified date April 2021
Source Poitiers University Hospital
Contact Nicolas LEVEZIEL, Pr
Phone 0549444182
Email nicolas.leveziel@chu-poitiers.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This goal of this study is to know the association between the central serous chorioretinopathy and the obstructive sleep apnea. Many studies have been done in order to assess the association between the central serous chorioretinopathy and obstructive sleep apnea and the results are always controverses actually.


Recruitment information / eligibility

Status Recruiting
Enrollment 70
Est. completion date August 6, 2021
Est. primary completion date August 6, 2021
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Central serous chorioretinopathy since 6 months at least - Patients beyond 18 years old Exclusion Criteria: - All retina pathology will be excluded : diabetes with affected retina, maculopathy, retina central veinous oclusion, epithéliopathy

Study Design


Locations

Country Name City State
France CHU de Poitiers Poitiers

Sponsors (1)

Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Association between central serous chorioretinopathy and the obstructive sleep apnea. Percentage of high risks of obstructive sleep apnea in patients affected by central serous chorioretinopathy in using the Berlin survey.
The Berlin questions include 3 categories:
The category 1 is positive if 2 answers are positive. The category 2 is positive if 2 answers are positive. The category 3 is positive if 1 answer is positive. Finally, if 2 categories are positive, the patient is considered as high risk of obstructive sleep apnea.
During 3 months we will collect the results of Berlin survey.
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