ltrasound guided percutaneous carpal tunnel release with hook blade

Phase 3

Completed

• Conditions: Carpal tunnel syndrome; Ultrasound guided; Percutaneous carpal tunnel release

• Registration Number: TCTR20170222006
• Lead Sponsor: on

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2017-02-22
• Study Completion: 2017-08-31
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 20

Inclusion Criteria

1. Carpal tunnel syndrome, onset more than 6 months
2. Confirm diagnosis with electrodiagnostic study

Exclusion Criteria

1. Previous carpal tunnel surgery
2. Other condition from ultrasound finding : carpal ganglion, mass lesion, tenosynovitis or synovial hypertrophy
3. Pregnancy
4. Bleeding tendency

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Function 0, 3 and 6 months Boston questionnaire carpal tunnel syndrome (score),Electrophysiologic improvement 0,3 and 6 months Electrodiagnostic study : Nerve conduction study (DSL, DML, CMAP amplitude),Morphologic change of median nerve 0, 3 and 6 months Ultrasound measurement of median nerve diameter (square millimaters)

Secondary Outcome Measures

Name	Time	Method
Patient satisfaction 3 months visual analog scale ,Return to work 2 weeks days,duration of pain killer medication use post procedure 2 weeks days