Single-port thoracoscopic sympathicotomy for treatment of complex regional pain syndrome type I, a feasibility study.

Completed

• Conditions: posttraumatic dystrophy; posttraumatic paindydrome; 10014982; 10009720

• Registration Number: NL-OMON36901
• Lead Sponsor: niversitair Medisch Centrum Groningen

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 29 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 20

Inclusion Criteria

CRPS-I refractory to standard treatment
Age 18-65 years

Exclusion Criteria

COPD > Gold I
>20 packyears smoking
Previous thoracic surgery on affected side

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Pain, measured in Visual Analoque Scale (VAS)-Score</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- Function in the extremity (RASQ-questionnaire and function tests)<br /><br>- Health Related Quality of Life (SF-36 questionnaire)</p><br>