Status:

COMPLETED

Syndactyly Versus Closed Reduction in 5th Metacarpal Neck Fracture

Lead Sponsor:

Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz

Conditions:

Metacarpal Fracture

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

This study aims to compare the functional results of two different therapeutic approaches in patients that present with a 5th metacarpal neck fracture. Patients will be randomly assigned to be treated...

Detailed Description

Syndactyly, although limiting the activity of the patient, allows a quick mobilization and recovery, as well as a better management in daily activities compared with immobilization with splint. In add...

Eligibility Criteria

Inclusion

  • Men and Women ≥ 18 years old.
  • Admitted to the Emergency Department with fracture of 5th metacarpal neck, in acute phase (maximum 72 h of evolution) with a possibility of clinical and radiological follow-up of at least 6 months.
  • Willing to participate in the study and give their consent in writing.

Exclusion

  • Patients younger than 18 years.
  • Patients presenting with more than 72 h of evolution
  • Patients with comminuted neck fractures.
  • Patients with angulation greater than 70 in the lateral-oblique plane
  • Patients with clinical-radiological disruption
  • Patients with previous fractures in the metacarpal.
  • Patients with open fracture grade II-III Gustilo.
  • Patients with bifocal fractures or fractures in another metacarpal-phalanx or carpal bones requiring different treatment.
  • Polytraumatized patients requiring further care that prevents them from adjusting to the therapeutic regimen specific to the protocol of isolated metacarpal fractures.
  • Patients with congenital anomalies on hand affect
  • Patients with a psychic disability (dementia-psychiatric illness or mental disorder) that prevents their collaboration in the follow-up
  • Patients with medical or surgical pathologies that at the discretion of the investigator do not allow their participation in the study.
  • Patients with inability to understand the nature and purpose of the study and / or to accept written participation in the study.
  • Unable to attend the pre-established clinical follow-up.
  • Do not wish to participate or give their consent in writing.

Key Trial Info

Start Date :

August 1 2016

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

January 31 2019

Estimated Enrollment :

72 Patients enrolled

Trial Details

Trial ID

NCT03434587

Start Date

August 1 2016

End Date

January 31 2019

Last Update

February 27 2019

Active Locations (1)

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Fundacion Jimenez Diaz

Madrid, Spain, 28040