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Comparing the Effects of Extracorporeal Shockwave Therapy and Splinting in the Treatment of Trigger Finger

Not Applicable
Not yet recruiting
Conditions
Trigger Finger
Shockwave Therapy
Registration Number
NCT06746974
Lead Sponsor
Mahidol University
Brief Summary

The goal of this study is to compare the effects of extracorporeal shockwave therapy and splinting in the treatment of trigger finger.

Participants will:

Be randomized into two groups (shockwave group and splint group). Visit the clinic once a week for four weeks for therapy. Keep a diary of their symptoms, which will be reviewed at six weeks.

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
24
Inclusion Criteria
  • Patients age ≥ 18 years
  • Grade I-III trigger finger patients (patients who has the presence of tenderness over the A1 pulley or painful locking or triggering as they fixed and extended the finger)
  • Patients who consented to participation in the study
Exclusion Criteria
  • Trigger thumb
  • The patients who had received previous treatment (steroid injection, ESWT or surgical release)
  • Patients with local infections, malignancies, severe coagulopathy and pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
100-mm. horizontal VAS scoreat enrollment, fourth week, and sixth week after first intervention

The VAS or Visual Analog Scale is a scale that is used to evaluate the level of pain. It is represented by a horizontal line that is 100-mm. long. The score is determined by measuring the distance in mm. A higher score on this scale indicates greater pain intensity.

Secondary Outcome Measures
NameTimeMethod
QuickDASH scoreat enrollment, fourth week, and sixth week after first intervention

The QuickDASH or Quick Disabilities of the Arm, Shoulder and Hand is a questionnaire that is used to evaluate the ability to perform activities of the arm, shoulder, and hand. It consists of 11 questions that patients are required to answer all of them. The answers are summarized in a range of 0-100, where a higher score indicates greater disability.

Number of triggeringat enrollment, fourth week, and sixth week after first intervention

The number of triggering events in ten active full fists will be scored out of ten. If a participant's finger remain locked at any time in making ten active full fists, they will be asked to stop and given a score of 10/10

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