Pain and patient-reported outcome associated with surgery for carpal tunnel syndrome or trigger finger under local anesthesia with and without tourniquet

Completed

• Conditions: Carpale tunnel syndroom, tenovaginitis stenosans; 1.) Carpal tunnel syndrome; median neuropathy. 2.) Stenosing tenosynovitis; trigger finger; 10034606

• Registration Number: NL-OMON48016
• Lead Sponsor: Jeroen Bosch Ziekenhuis

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Completion: 2021-08-10
• Last Update Posted: 15 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 142

Inclusion Criteria

Operative treatment for carpal tunnel syndrome or stenosing tenosynovitis

Exclusion Criteria

Coagulopathy or use of vitamin K antagonist that may not be temporary withdrawn
Recurrent or persisting CTS or TVS
Axillary lymph node dissection of the affected limb

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Pain during the surgery on a 0-10 numeric rating scale</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>Patient-reported outcome measures:<br /><br>- QuickDASH<br /><br>- BCTQ<br /><br>- Postoperative complications</p><br>