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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05531929
Other study ID # 8614
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 22, 2022
Est. completion date December 22, 2022

Study information

Verified date December 2023
Source University Hospital, Strasbourg, France
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Anxiety-depressive disorders are also very frequent, in the form of different pathologies that are often intertwined (prevalence of generalized anxiety disorders in 5% of the population, characterized depressive episodes in 5%, etc.). And it is even more frequent in patients with a cuff tendinopathy (26% and 23% of depression and anxiety respectively). These 2 pathologies are therefore responsible for significant economic expenses. It is in this context that the investigators' wish to carry out this study seems justified in order to better understand and therefore manage this problem, which is frequently encountered in daily practice and which would therefore allow better understanding and therefore better information for the patients concerned.


Recruitment information / eligibility

Status Completed
Enrollment 212
Est. completion date December 22, 2022
Est. primary completion date October 22, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion criteria: - Major subject (= 18 years) - Operated between January 2008 and September 2009 arthroscopically for a symptomatic supraspinatus tendon rupture, retracted in zone 1, resistant to medical treatment with a mobile shoulder, fatty degeneration of stage 2 or less with also a preserved subacromial space - Subject not objecting to the reuse of their data for scientific research purposes. Exclusion criteria: - Subject having expressed his opposition to the reuse of his data for scientific research purposes.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
France Service de Chirurgie orthopédique de l'épaule et du coude - CHU de Strasbourg - France Strasbourg

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Strasbourg, France

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Measurement of the duration of complete sports cessation after rotator cuff repair surgery 6 months after rotator cuff repair surgery
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