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NCT06137404 Clinical Trial

A Comparison of Metacarpophalangeal Joint Blocking Splint With Relative Motion Extension Splint for Trigger Finger

Trigger Finger Clinical Trial

Official title:
A Comparison of Metacarpophalangeal Joint Blocking Splint With Relative Motion Extension Splint for Trigger Finger

Clinical Trial Details — Status: Enrolling by invitation

Administrative data
NCT number NCT06137404
Other study ID # WaikatoH
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date March 1, 2022
Est. completion date March 31, 2028

Study information
Verified date October 2023
Source Waikato Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of this research is to evaluate the effectiveness of two splint designs in conservative management of trigger finger.

Description:

This study aims to analyse and compare the effectiveness of metacarpophalangeal joint blocking splint versus relative motion extension splint for trigger finger. This will help us find out which one of the two splint designs is more effective in the management of trigger finger, thus improving treatment outcomes for patients with trigger finger.

Recruitment information / eligibility
Status Enrolling by invitation
Enrollment 30
Est. completion date March 31, 2028
Est. primary completion date March 31, 2026
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Trigger finger patient Exclusion Criteria: - Diabetes, non-English speaking

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• Splint
Comparison of splints for trigger finger

Locations
Country Name City State
New Zealand Waikato Hospital Hamilton Waikato

Sponsors (1)
Lead Sponsor Collaborator
Waikato Hospital

Country where clinical trial is conducted

New Zealand, 

Outcome
Type Measure Description Time frame Safety issue
Other Visual Analogue Scale (VAS) The VAS is a patient rated outcome measure that enables the patient to rate the intensity of pain from 0 (no pain) to 10 (worse pain that can possibly be) 12 weeks
Primary Green's classification for trigger finger Green's classification is an objective outcome measure. The therapist grades the triggering by observing the finger when the patient makes a full fist.
Grade I: Pain/history of catching Grade II: Demonstrable catching but can actively extend digit Grade III: Demonstrable locking, requiring passive extension Grade IV: Fixed flexion contracture
Lowest score is I; highest score is IV		 12 weeks
Secondary QuickDASH (Disability of Arm, Shoulder and Hand) The QuickDASH is a patient rated questionnaire that rates patient's ability to perform certain tasks as well as severity of symptoms. The best score is 0 (no difficulty) and the lowest score is 100 (severe difficulty). 12 weeks
See also
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Active, not recruiting NCT01886157 - Treatment of Trigger Finger With Steroid Injection Versus Steroid Injection and Splinting N/A
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