Efficacy of Ultrasound-Guided Hydrodissection in Carpal Tunnel Syndrome

NCT05222126 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2024-01-11

No results posted yet for this study

Summary

The aim of our study is to determine the effectiveness of US-guided hydrodissection of the median nerve in different contents and volumes in patients diagnosed with mild to moderate carpal tunnel syndrome.

Conditions

  • Musculoskeletal Diseases
  • Median Nerve Disease
  • Carpal Tunnel Syndrome
  • Ultrasound-Guided Injection

Interventions

PROCEDURE

Ultrasound-guided Hydrodissection (HD) with 5 cc 5% Dextrose

The median nerve will be defined at the proximal entrance of the carpal tunnel (scaphoid-pisiform plane). Under the ulnar approach with the in-plane technique, first it was planned to hydrodissect the median nerve from the retinaculum superiorly and then from the flexor tendons inferiorly, using 5 cc of 5% dextrose.

PROCEDURE

Ultrasound-guided Hydrodissection (HD) with 5 cc Normal Saline

The median nerve will be defined at the proximal entrance of the carpal tunnel (scaphoid-pisiform plane). Under the ulnar approach with the in-plane technique, first it was planned to hydrodissect the median nerve from the retinaculum superiorly and then from the flexor tendons inferiorly, using 5 cc normal saline.

PROCEDURE

Ultrasound-guided Hydrodissection (HD) with 10 cc 5% Dextrose

The median nerve will be defined at the proximal entrance of the carpal tunnel (scaphoid-pisiform plane). Under the ulnar approach with the in-plane technique, first it was planned to hydrodissect the median nerve from the retinaculum superiorly and then from the flexor tendons inferiorly, using 10 cc 5% dextrose.

PROCEDURE

Ultrasound-guided Hydrodissection (HD) with 10 cc Normal Saline

The median nerve will be defined at the proximal entrance of the carpal tunnel (scaphoid-pisiform plane). Under the ulnar approach with the in-plane technique, first it was planned to hydrodissect the median nerve from the retinaculum superiorly and then from the flexor tendons inferiorly, using 10 cc normal saline.

Sponsors & Collaborators

  • Afyonkarahisar Health Sciences University

    lead OTHER

Principal Investigators

  • Nuran EYVAZ, MD · Afyonkarahisar Health Sciences University

  • Ali İzzet AKÇİN, MD · Afyonkarahisar Health Sciences University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
20 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-20
Primary Completion
2023-12-20
Completion
2024-01-10

Countries

  • Turkey (Türkiye)

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 NCT05222126 on ClinicalTrials.gov