Satisfaction and Recovery After Trigger Finger Release
TH III
1 other identifier
observational
110
1 country
1
Brief Summary
Trigger finger release is one of the most common procedures in hand surgery. However, little is known about the patient perceived outcome directly after surgery and the timespan to recovery of normal hand function.This study focuses on patient reported outcome scores within the first six weeks after surgery.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Apr 2022
Typical duration for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 6, 2022
CompletedFirst Posted
Study publicly available on registry
April 20, 2022
CompletedStudy Start
First participant enrolled
April 26, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 26, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
November 26, 2024
CompletedNovember 27, 2024
November 1, 2023
2.6 years
April 6, 2022
November 26, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Self-assessed hand function
change in total score of hand-specific questionnaire (HAKIR) week by week. Best score 100, worst 0
every week for 6 weeks
Secondary Outcomes (3)
Pain (assessed by patient)
6 weeks
Movement of finger (self-assessed by patient)
6 weeks
Frequency of trigger phenomenon (self-assessed by patient)
6 weeks
Interventions
The A1 pulley and tendon sheath is divided in local anaestethic through a small incision in the palm
Eligibility Criteria
Patient scheduled for trigger finger release
You may qualify if:
- Trigger phenomenon and/or
- Tenderness volarly to MCP joint of affected finger/thumb
- Patient scheduled for trigger finger release
- Signed informed consent
You may not qualify if:
- Concomitant hand injuries/ conditions
- Multiple fingers/thumbs to be treated
- Unable to read/understand instructions in Swedish
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Alingsås lasarett
Alingsås, Sweden
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- senior consultant surgeon, MD, PhD
Study Record Dates
First Submitted
April 6, 2022
First Posted
April 20, 2022
Study Start
April 26, 2022
Primary Completion
November 26, 2024
Study Completion
November 26, 2024
Last Updated
November 27, 2024
Record last verified: 2023-11