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OpenTrials
Completed

NCT Number: NCT05426473

Differences in Quality of Life After Thoracic Outlet Syndrome Surgery

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

Completed

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University Hospital

Angers, France

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

QuickDASH form

Other

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

Other names: SF-36 form

Primary outcomes

  1. Change from QuickDASH form results before surgery at 6 weeks after surgery

    Time frame: Results before surgery and at 6 weeks after surgery are compared

Secondary outcomes

  1. Change from SF-36 form results before surgery at 6 weeks after surgery

    Time frame: Results before surgery and at 6 weeks after surgery are compared

Sponsors and collaborators

Lead sponsor

University Hospital, Angers

Other Gov

Registry information

Acronym: POST-AP

Important dates

Study start
2022
Primary completion
2024
Study completion
2024
First posted
Jun 22, 2022
Registry last updated
Aug 14, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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