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NCT05024617 Clinical Trial

Stage-Specific Recovery Changes in the International Classification of Functioning Components Following Conservative Rehabilitation of Trigger Finger

Trigger Finger Clinical Trial

Official title:
Stage-Specific Recovery Changes in the International Classification of Functioning Components Following Conservative Rehabilitation of Trigger Finger

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05024617
Other study ID # 16969557-437
Secondary ID
Status Completed
Phase
First received
Last updated
Start date March 2, 2019
Est. completion date August 31, 2019

Study information
Verified date August 2021
Source Hacettepe University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The aim of this study was to determine the effectiveness of conservative rehabilitation on the multi-dimensional health components based on WHO ICF model in Stage 1, Stage 2 and Stage 3 trigger finger and to determine the functional recovery patterns of each dimension during a three-month rehabilitation period. Thirty-four patients were participated in the study.

Recruitment information / eligibility
Status Completed
Enrollment 34
Est. completion date August 31, 2019
Est. primary completion date May 20, 2019
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 35 Years to 65 Years
Eligibility Inclusion Criteria: - Diagnosed with Stage 1, Stage 2 and Stage 3 trigger finger based on the Froimson Classification Exclusion Criteria: - Paediatric trigger finger, trigger thumb, concomitant de'Quervain tenosynovitis, carpal tunnel syndrome, or Dupuytren's contracture, neurological or rheumatological diseases, chronic pain syndromes, pregnancy and patients with treatment history of related finger/fingers.

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• conservative treatment
All patients had rehabilitation for a total of three months, including activity modification, splinting and exercises.

Locations
Country Name City State
Turkey Hacettepe University Faculty of Physical Therapy and Rehabilitation Ankara

Sponsors (1)
Lead Sponsor Collaborator
Hacettepe University

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Pain (VAS) one month
Primary Number of triggering (ten active fist test / 30 second active fist test) one month
Primary Grip strength (hand dynomometer and pinchmeter) one month
See also
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Completed NCT01987115 - Comparison of Fascial Manipulation With Traditional Physiotherapy for the Treatment of Trigger Fingers N/A
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Completed NCT01950793 - A Comparison Between Sonoguided Injection Corticosteroid and Hyaluronic Acid Injection in Treatment of Trigger Finger N/A
Recruiting NCT04675892 - Resection of Flexor Digitorum Superficialis Tendon for Severe Trigger Fingers N/A
Terminated NCT05082480 - Evaluate the Effectiveness of Crosslinked HA on the Adhesion Preventing After Trigger Finger Release Surgery N/A
Recruiting NCT05045157 - Effectiveness of Percutaneous Pulley Release With Infiltration, Versus Infiltration Alone in Trigger Finders N/A
Active, not recruiting NCT01886157 - Treatment of Trigger Finger With Steroid Injection Versus Steroid Injection and Splinting N/A
Recruiting NCT00951236 - Study Comparing One Versus Two Cortisone Injections for Trigger Finger N/A
Withdrawn NCT04855942 - Focused Extracorporeal Shock Wave Therapy (ESWT) Versus Traditional Physiotherapy in the Treatment of Trigger Finger N/A