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Clinical Routine in Thoracic Outlet Syndrome

NCT04376177 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2021-06-03

No results posted yet for this study

Summary

Transversal recording and analysis of investigations performed in patients referred for suspected thoracic outlet syndrome (TOS)

Conditions

  • Thoracic Outlet Syndrome

Interventions

DIAGNOSTIC_TEST

Ultrasound

Echodoppler imaging of upper limbs performed by trained operators at rest and during provocative maneuvers for TOS diagnosis.

DIAGNOSTIC_TEST

angiography

Angiography (arterial and/or venous) of upper limbs performed by trained operators at rest and during provocative maneuvers such for TOS diagnosis.

DIAGNOSTIC_TEST

questionnaires

Use of standard questionnaires (MASC, DASH, SF36) for the evaluation of upper limb symptoms self-completed by the patients at admission.

DIAGNOSTIC_TEST

Transcutaneous oximetry

Mesurement of transcutaneuos oxygen pressure on both forearms performed at rest and during provocative maneuversfor TOS diagnosis.

DIAGNOSTIC_TEST

plethysmography

Photoplethysmography of the forearms or fingers performed at rest and during provocative maneuvers for TOS diagnosis

DIAGNOSTIC_TEST

Electromyogram

Electromyography of the upper limbs with encoding of the physician for the presence or abnsence of signs of plexis compression (impairment of the response on C8 T1 erea

DIAGNOSTIC_TEST

Standard X-Ray

Standard X-Ray performed for the research of apophysomegaly or additionnal cervical rib.

Sponsors & Collaborators

  • University Hospital, Angers

    lead OTHER_GOV

Principal Investigators

  • Pierre ABRAHAM, MD; PhD · University and univerity hospital in Angers, FRANCE

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-01-01
Primary Completion
2025-12-31
Completion
2025-12-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04376177 on ClinicalTrials.gov