NCT03928873

Extracorporeal Shock Wave in the Treatment of Trigger Finger

Extracorporeal Shock Wave Therapy Versus Placebo in the Treatment of Trigger Finger: a Randomized Controlled Study
Taipei Medical University WanFang Hospital·ClinicalTrials.gov·device·Device trial
View on ClinicalTrials.gov
Study focus
Disease/Condition
Trigger Finger
Drug/Device/Intervention
Low energy ESWT
Study type
Interventional
Intervention type
device
Sponsor & location
Primary sponsor
Taipei Medical University WanFang Hospital
Location
Taipei, Taiwan
Timeline & enrollment
Phase
N/A
Start date
Feb 20, 2019
End date
Nov 22, 2019
Enrollment
60 participants
Primary outcome

The efficacy of ESWT in the treatment of trigger finger

Summary

Trigger finger (TF) is a condition that causes triggering, snapping, or locking on flexion of
 the involved finger, with a life- time risk between 2%-3% in the general population. A
 variety of treatments have been described, but the most effective treatment for this common
 disorder is still under debate. Recently, extracorporeal shock wave therapy(ESWT) has been
 advanced as a possible alternative to surgery for the treatment of musculoskeletal disorders
 in patients recalcitrant to traditional conservative treatment.
 
 However, the effectiveness of ESWT on the treatment of TF is still in lack of evidence. The
 purpose of this study is to conduct a prospective randomized clinical trial to compare the
 efficacies of ESWT at two different energy flux density with placebo treatment for the
 management of TF. The investigators intended to enrolled 60 participants randomly allocated
 to three groups: low energy ESWT (1500 impulses and 0.006mJ/mm2, 3bar, once per week for 4
 weeks), high energy ESWT (1500 impulses and 0.01mJ/mm2, 5.8bar, once per week for 4 weeks) or
 placebo treatment groups. The effectiveness of the treatment will be assessed using cure
 rates, a visual analogue scale, the frequency of triggering, the severity of triggering, the
 functional impact of triggering, and the Quick-Disabilities of the Arm, Shoulder, and Hand
 questionnaire (qDASH) at 1, 3, and 6 months after treatment. An intention-to-treat analysis
 will be used in this study. The investigators intend to determine the efficacy of ESWT in the
 treatment of TF and to find out the ideal energy set-up of ESWT for TF treatment.

ICD-10 classifications
Trigger fingerAccessory finger(s)Fused fingersAccessory thumb(s)Clubbing of fingers
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT03928873
Type
Device Trial
About this record

Access comprehensive clinical trial information for NCT03928873 through Pure Global AI's free database. This phase not specified trial is sponsored by Taipei Medical University WanFang Hospital and is currently status unknown. The study focuses on Trigger Finger. Target enrollment is 60 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.