Skip to main content
Clinical Trials/NCT06398483
NCT06398483RecruitingNot Applicable

Comparative Study Between Micro Plate Fixation and Blocking k.Wire in Management of Acute Bony Mallet Finger : Randomized Controlled Clinical Trial Study

Sohag University1 site in 1 country20 target enrollmentStarted: April 25, 2024Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Recruiting
Enrollment
20
Locations
1
Primary Endpoint
post operative evalution of management of acute bony mallet finger

Study Overview

Brief Summary

Mallet finger is an avulsion fracture of the distal phalanx or rupture of the extensor terminal band caused by distal interphalangeal (DIP) joint hyperflexion or axial loading. In the treatment of mallet finger fractures, surgical repair is recommended in cases where the fracture involves more than one-third of the distal phalanx joint surface or the distal phalanx becomes volar subluxated

The blocking k.wire and micro plate technique are some of the methods used in the treatment of mallet finger fractures In recent years, the blocking k.wire technique has gained popularity owing to its minimally invasive nature and its ability to achieve satisfactory postoperative results

The main advantages of Micro Plate technique include provision of anatomical reduction and stable fixation, avoiding the risk of fragmentation of the small dorsal fragment, allowing early movement and increasing patient comfort and compliance

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
None

Eligibility Criteria

Sex
All
Accepts Healthy Volunteers
Yes

Inclusion Criteria

  • Acute bony mallet finger involves more than one third of the distal phalanx joint surface or the distal phalanx becomes volar sublaxed

Exclusion Criteria

  • 1- . crushed distal phalanx
  • soft tissue mallet
  • multiple phalangeal fractures
  • old neglected cases

Outcomes

Primary Outcomes

post operative evalution of management of acute bony mallet finger

Time Frame: 6 months

Clinical evaluation of improvement of pain , deformity , range of motion , incidence of surgical site infection , radiographic union time

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Mostafa Ahmed Mohamed Elsadik

Resident at orthopedics and trauma surgery department

Sohag University

Study Sites (1)

Loading locations...

Similar Trials