Mode
Text Size
Log in / Sign up
N/A N=46 Randomized Double-blind Treatment

Continuous And Pulsed Ultrasound Treatments On Carpal Tunnel Syndrome

Carpal Tunnel Syndrome

Enrolled (actual)
46
Serious AEs
0.0%
Results posted
Nov 2023
Primary outcome: Primary: Change From Baseline in Symptom Severity With Symptom Severity Scale — 23.06; 22.06; 19.66 units on a scale — p=0.442

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
ultrasound (Device); pulsed ultrasound (Device); placebo ultrasound (Device)
Age
Pediatric, Adult, Older Adult
Sex
Female
Sponsor
Eskisehir Osmangazi University
Primary completion
Jun 2013

Outcome Measures

OutcomeResultp-value
PRIMARY
Change From Baseline in Symptom Severity With Symptom Severity Scale
23.06; 22.06; 19.66 0.442
SECONDARY
Change From Baseline in Pain With Visual Analogue Scale
4.40; 2.68; 3.53 0.083
SECONDARY
Change From Baseline in Functional Status With Functional Status Scale
18.8; 19.31; 14.2 0.125
SECONDARY
Changes From Baseline Nervus Medianus Motor Conduction Velocity
54.26; 55.68; 57.91 0.146

Summary

The aim of this placebo-controlled study was to evaluate the effects of pulsed and continuous ultrasound treatments combined with splint therapy on patients with mild and moderate idiopathic carpal tunnel syndrome

Eligibility Criteria

Inclusion Criteria

  • Mild or moderate idiopathic carpal tunnel syndrome (without thenar atrophy or spontaneous activity on electrophysiological examination of the abductor pollicis brevis (APB) muscle)

Exclusion Criteria

  • Secondary entrapment neuropathies
  • Cervical radiculopathy
  • Systemic diseases with increased risk of the carpal tunnel syndrome
  • Gained surgical relief of the syndrome
  • Treated with ultrasound for the syndrome
  • A history of steroid injections into the carpal tunnel and of physical therapy within the last 3 months
  • Patients with either thenar atrophy or spontaneous activity (fibrillation potentials and positive sharp waves) on electrophysiological examination
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02054247). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search