Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT07357493

metaCARpal Bone Osteosynthesis Trail

Led by Karolinska Institutet · Updated on 2026-03-24

552

Participants Needed

1

Research Sites

259 weeks

Total Duration

On this page

Sponsors

K

Karolinska Institutet

Lead Sponsor

U

Uppsala University

Collaborating Sponsor

AI-Summary

What this Trial Is About

Background Metacarpal shaft fractures account for 30-50% of hand fractures (Karl et al., 2015; Kollitz et al., 2014; van Onselen et al., 2003), with diaphyseal spiral and oblique fractures of the second to fifth ray posing unique challenges due to the risks of shortening and rotational deformities. Current standard care of displaced fractures involves operative fixation. However, retrospective studies have indicated that nonoperative treatment, involving early mobilization or buddy taping, can achieve outcomes comparable to operative treatment (Daher et al., 2023). There is only one published, with a small sample size, randomized controlled trial (RCT) investigating this issue (Peyronson et al., 2023). This highlights the need for a robust multicenter RCT to address these gaps in evidence. Aim The aim of this study is to compare the one-year outcomes of non-operative treatment involving immediate unrestricted mobilization versus operative treatment of displaced oblique or spiral diaphyseal metacarpal fractures in adults. Materials and Methods This is a multicenter, pragmatic, prospective, noninferiority RCT involving 552 adult patients with displaced oblique and/or spiral diaphyseal metacarpal fractures of the second to fifth ray. Participants will be randomized 1:1 to receive either nonoperative treatment with unrestricted mobilization and rehabilitation) or operative treatment (with screw or plate fixation) followed by rehabilitation. The primary outcome is grip-strength in the injured hand presented in kilograms at one year. Secondary outcomes include questionnaires, complications, range of motion, patient reported outcome measures, health related quality of life, patient satisfaction, and radiographic healing. A power calculation proposes a study size of 552 participants to detect a noninferiority margin of 10% in grip strength.

CONDITIONS

Official Title

metaCARpal Bone Osteosynthesis Trail

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age 6518 years
  • Access to a valid e-mail
  • Injury within 10 days prior to inclusion
  • Normal bilateral hand function prior to injury
  • Ability and willingness to provide written informed consent
  • Single, displaced spiral or oblique diaphyseal fracture of the second to fifth metacarpals with fracture line length at least twice the diameter of the bone
  • Fractures with at least 2 mm of radiological displacement and/or malrotation of injured finger compared to uninjured side
Not Eligible

You will not qualify if you...

  • Expected difficulty adhering to the study protocol (e.g., due to insufficient language proficiency, dementia, substance abuse, or other reasons)
  • Presence of open fracture with Gustilo-Anderson grade greater than I or pathological fracture
  • Presence of ipsilateral fracture of the upper extremity, polytrauma, or generalized joint dysfunction such as rheumatoid arthritis

AI-Screening

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Trial Site Locations

Total: 1 location

1

Karolinska Institutet, Danderyd's hospital

Stockholm, Stockholm County, Sweden, 18288

Actively Recruiting

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Research Team

C

Cecilia Mellstrand Navarro, Associate professor

CONTACT

E

Elsa Pihl, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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metaCARpal Bone Osteosynthesis Trail | DecenTrialz