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Clinical Trials/NCT05336045
NCT05336045CompletedNot Applicable

Satisfaction and Recovery After Trigger Finger Release- a Prospective Cohort Study With Weekly PROMs

Sahlgrenska University Hospital, Sweden1 site in 1 country110 target enrollmentStarted: April 26, 2022Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
110
Locations
1
Primary Endpoint
Self-assessed hand function

Study Overview

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.

Detailed Description

Patients scheduled for release of trigger finger are assessed regarding the following outcome measures:

  1. VAS score for pain
  2. VAS score for finger movement
  3. VAS score for fréquence of triggering
  4. HAKIR questionnaire (validated instrument for hand function in the Swedish national hand registry)
  5. Quick-DASH questionnaire.

After surgery, the patients records the following outcomes:

Each day: 1,2,3 and records of pain medication details Each week: 4,5

for 6 weeks

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Trigger phenomenon and/or
  • Tenderness volarly to MCP joint of affected finger/thumb
  • Patient scheduled for trigger finger release
  • Signed informed consent

Exclusion Criteria

  • Concomitant hand injuries/ conditions
  • Multiple fingers/thumbs to be treated
  • Unable to read/understand instructions in Swedish

Outcomes

Primary Outcomes

Self-assessed hand function

Time Frame: every week for 6 weeks

change in total score of hand-specific questionnaire (HAKIR) week by week. Best score 100, worst 0

Secondary Outcomes

  • Frequency of trigger phenomenon (self-assessed by patient)(6 weeks)
  • Pain (assessed by patient)(6 weeks)
  • Movement of finger (self-assessed by patient)(6 weeks)

Investigators

Sponsor
Sahlgrenska University Hospital, Sweden
Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Joakim Stromberg

senior consultant surgeon, MD, PhD

Sahlgrenska University Hospital, Sweden

Study Sites (1)

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