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Enrolling by invitation NCT06137404

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

No phase Interventional Trigger Finger

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Splint.
Who it may be relevant to
Registry conditions: Trigger Finger. Basic parameters: No limits · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
New Zealand
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

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

Detailed 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.

Interventions

  • Other Splint
    Comparison of splints for trigger finger

Primary outcome measures

  • Green's classification for trigger finger [Time frame: 12 weeks]
Secondary outcome measures (1)
  • QuickDASH (Disability of Arm, Shoulder and Hand) [Time frame: 12 weeks]

Eligibility criteria

Inclusion criteria

  • Trigger finger patient

Exclusion criteria

  • Diabetes, non-English speaking

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Single group
Masking
Triple blind
Primary purpose
Treatment

Study locations

New Zealand · 1 center
  • Waikato Hospital — Hamilton

Identifiers

NCT: NCT06137404 · WaikatoH

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗