Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
NCT04574336

Scandinavian Humeral Diaphyseal Fracture Trial

Led by Kolding Sygehus · Updated on 2024-04-16

287

Participants Needed

22

Research Sites

486 weeks

Total Duration

On this page

Sponsors

K

Kolding Sygehus

Lead Sponsor

C

Copenhagen University Hospital, Hvidovre

Collaborating Sponsor

AI-Summary

What this Trial Is About

This pragmatic multicenter randomized controlled trial (RCT) includes adult participants with an acute humeral shaft fracture to compare surgical fixation of humeral shaft fracture to non-surgical treatment with early identification and treatment of delayed union by a patient-reported outcome after 52 weeks. The trial population of 287 participants The trial population is divided in two age-groups due to the changes in DASH score by age. The definition of delayed union differs in the young and elderly population to consider dissimilarity in bone healing rates and the timepoint for crossover is therefor different between the groups. Participants will be randomized 1:1 between non-surgical treatment and surgical treatment. The primary outcome is the Disability of Arm, Shoulder and Hand (DASH) score at 52 weeks, and is assessor blinded. The secondary outcomes are DASH score earlier than 52 weeks, EQ-5D-5L, pain assessed by visual analogue score, Constant-Murley score including elbow range of motion and anchor-questions collected at all timepoints throughout the trial. All complications will be reported including; infection, nerve or vascular injury, surgical revisions (implant malpositioning, hardware failure, aseptic loosening and peri-implant fracture), major adverse cardiovascular events, other major adverse events and mortality. SHAFT will provide information on the effectiveness of two standard treatments for humeral shaft fractures, while taking the dilemmas within the population into account.

CONDITIONS

Official Title

Scandinavian Humeral Diaphyseal Fracture Trial

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Fracture types 12A-C according to OTA/AO classification
  • Includes minimally displaced extra-articular fractures extending to the proximal humerus (less than 1 cm displacement or 45 degrees angulation)
  • Treatment must start within 14 days of trauma
  • Age 18-64 years for younger group (SHAFT-Y) or 65 years and older for elderly group (SHAFT-E)
  • Ability to understand and speak Danish, Swedish, or Norwegian to complete study paperwork
Not Eligible

You will not qualify if you...

  • Unable to give informed consent
  • Undisplaced shaft fractures (less than cortex-wide displacement in all radiographic planes)
  • Vascular injury in the arm on the same side as the fracture
  • Polytrauma with additional fractures or urgent surgical needs
  • Pathological fractures
  • Open fractures
  • Body mass index over 40
  • Health conditions that prevent either surgical or non-surgical treatment
  • Fractures involving distal humerus or displaced proximal humerus extensions
  • Isolated fractures of proximal or distal humerus

AI-Screening

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Trial Site Locations

Total: 22 locations

1

Aabenraa Hospital

Aabenraa, Denmark

Actively Recruiting

2

Aarhus Hospital

Aarhus, Denmark

Actively Recruiting

3

Bispebjerg Hospital

Copenhagen, Denmark

Actively Recruiting

4

Hvidovre Hospital

Copenhagen, Denmark

Actively Recruiting

5

Esbjerg Hospital

Esbjerg, Denmark

Actively Recruiting

6

Aalborg-Farsø Hospital

Farsø, Denmark

Actively Recruiting

7

Herlev-Gentofte Hospital

Gentofte Municipality, Denmark

Actively Recruiting

8

New North Zealand Hospital

Hillerød, Denmark

Actively Recruiting

9

Holbæk Hospital

Holbæk, Denmark

Actively Recruiting

10

Kolding Hospital

Kolding, Denmark

Actively Recruiting

11

Zealand University

Køge, Denmark, 4600

Actively Recruiting

12

Odense Hospital

Odense, Denmark

Actively Recruiting

13

Slagelse Hospital

Slagelse, Denmark

Actively Recruiting

14

Viborg Regional Hospital

Viborg, Denmark, 8000

Actively Recruiting

15

Helsinki University Hospital

Helsinki, Finland

Actively Recruiting

16

Tampere University Hospital

Tampere, Finland

Actively Recruiting

17

Oslo University Hospital (Ullevål)

Oslo, Norway

Actively Recruiting

18

Stanvanger University Hospital

Stavanger, Norway

Actively Recruiting

19

Danderyd University Hospital

Stockholm, Sweden

Actively Recruiting

20

Karolinska University Hospital

Stockholm, Sweden

Actively Recruiting

21

Umeå University Hospital

Umeå, Sweden

Actively Recruiting

22

Uppsala University Hospital

Uppsala, Sweden

Actively Recruiting

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Research Team

D

Dennis Karimi, M.D

CONTACT

B

Bjarke Viberg, MD, 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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