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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05426473
Other study ID # 2022-A01379-34
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 5, 2022
Est. completion date August 17, 2026

Study information

Verified date October 2022
Source University Hospital, Angers
Contact Eva Deveze, Dr
Phone 0686450820
Email Eva.Deveze@chu-angers.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Quality of life evaluation after thoracic outlet surgery with Quick-DASH and SF-36 forms


Recruitment information / eligibility

Status Recruiting
Enrollment 112
Est. completion date August 17, 2026
Est. primary completion date March 14, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - thoracic outel syndrome surgery scheduled in the vascular and thoracic surgery department of Angers ; age > 18 y ; french language understood Exclusion Criteria: - denied of consent

Study Design


Related Conditions & MeSH terms


Intervention

Other:
QuickDASH form
Patients have to complete these two forms, Quick DASH and SF-36, before surgery then 6 weeks after

Locations

Country Name City State
France University Hospital Angers

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change from QuickDASH form results before surgery at 6 weeks after surgery Results before surgery and at 6 weeks after surgery are compared
Secondary Change from SF-36 form results before surgery at 6 weeks after surgery Results before surgery and at 6 weeks after surgery are compared
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