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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04771039
Other study ID # HRIPH
Secondary ID
Status Completed
Phase
First received
Last updated
Start date January 1, 2013
Est. completion date December 12, 2020

Study information

Verified date December 2020
Source Central Hospital, Nancy, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Ocular damage is found in the 3rd rank of extra intestinal manifestations (MEI) Potentially serious functional complications (see uveitis and risk of blindness) requiring rapid management Rare uveitis in the literature (0.5% -3%), study on a large sample to assess their prevalence in patients with IBD at the Nancy CHRU and describe all the ocular manifestations that can be found.


Recruitment information / eligibility

Status Completed
Enrollment 87
Est. completion date December 12, 2020
Est. primary completion date December 1, 2020
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adult patients followed at Nancy University Hospital for IBD and having consulted in the ophthalmology department Exclusion Criteria: - Minor patients - patients without IBD - patients for whom there is no ophthalmology consultation

Study Design


Intervention

Other:
reason for consultation
search in medical files for reasons for ophthalmology consultation, functional signs, clinical signs, treatment, characteristics of IBD

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Central Hospital, Nancy, France

Outcome

Type Measure Description Time frame Safety issue
Primary frequency frequency of ocular manifestations in inflammatory bowel disease baseline
Secondary Number Number of uveitis, scleritis and episcleritis; prevalence calculation baseline
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