MedPath

Comparison of New Suture Anchor Technique for Bony Mallet Injury Versus Conservative Treatment

Not Applicable
Completed
Conditions
Finger Injuries
Finger Fracture
Finger Mallet
Interventions
Procedure: Suture anchor technique
Procedure: Conservative Treatment
Registration Number
NCT03228849
Lead Sponsor
Istanbul University
Brief Summary

This study aims to compare conservative treatment versus a new suture anchor technique for bony mallet finger in 29 patients.

Detailed Description

This study aims to compare conservative treatment versus a new suture anchor technique for bony mallet finger in 29 patients who presented to investigators' clinic between 2013 and 2015. Patients were randomly assigned to conservative or surgical treatment groups. Patients in the conservative group were followed with immobilization with aluminum splint and physical therapy. Patients in the surgical group were treated with investigators' new surgical suture anchor technique and then received physical therapy. The patients were followed for 12 months. Primary study outcomes were extension deficit, days to return to work and DIP flexion.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
29
Inclusion Criteria
  • Wehbe Schneider type 1 - 2 and type A - B fractures
  • ability to provide closed reduction
  • patients' voluntariness
Exclusion Criteria
  • Wehbe Schneider type C and type 3 fractures

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Surgical TreatmentSuture anchor techniquePatients were treated with the new suture anchor technique and after 6 weeks were started on physical therapy for 2 weeks.
Conservative TreatmentConservative TreatmentPatients were treated with 6 weeks with splinting and were then started on physical therapy for 2 weeks.
Primary Outcome Measures
NameTimeMethod
Extension deficit12 months

The inability to actively extend DIP joint to 0 degrees.

DIP flexion12 months

The maximum angle of flexion at DIP joint

Days to return to workStarting from the date of the start of treatment until patients returns to work, assessed up to 12 months

Time to return to work

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Istanbul University Faculty of Medicine

🇹🇷

Istanbul, Turkey

© Copyright 2025. All Rights Reserved by MedPath