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CompletedNCT05426473POST-APUpdated Aug 14, 2025

Differences in Quality of Life After Thoracic Outlet Syndrome Surgery

An interventional study of QuickDASH form in Thoracic Outlet Syndrome, sponsored by University Hospital, Angers. Completed at 1 site in France. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-08-14.

Sponsored by University Hospital, Angers · Not applicable, Interventional, and Supportive care

Phase
Not applicable
Study type
Interventional
Enrollment
88
Allocation
Not applicable
Ages
18 Years and older
Sex
All
01

Study summary

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

02

Conditions studied

  • Thoracic Outlet Syndrome
03

In context

Thoracic Outlet Syndrome

33 studies on the registry are indexed under Thoracic Outlet Syndrome; 12 are open to participants now.

This study's enrollment of 88 is above the median of 50 across 17 interventional studies indexed under Thoracic Outlet Syndrome.

Browse Thoracic Outlet Syndrome studies →

Lead sponsor

University Hospital, Angers is the lead sponsor of 464 studies on the registry; 116 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • thoracic outel syndrome surgery scheduled in the vascular and thoracic surgery department of Angers ; age > 18 y ; french language understood

Exclusion criteria

Exclusion Criteria:

  • denied of consent
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Not applicable
Intervention model
Single group
Masking
None (open label)
Enrollment
88 participants (actual)

Study arms

  • Experimental
    Patients with a completed form

    Other: QuickDASH form

Interventions

  • OtherQuickDASH form

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

    Also known as: SF-36 form

06

What researchers measure

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

07

Study locations

1 site
  • University Hospital
    Angers, France
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 14, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05426473
Lead sponsor
University Hospital, Angers
Responsible party
Sponsor
First posted
Jun 22, 2022
Start date
Sep 5, 2022
Primary completion
Jan 8, 2024
Completion
Jan 8, 2024
Last update
Aug 14, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Aug 2025. You cannot join it, but the record below documents what was studied.

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Discussion

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