Scandinavian Humeral Diaphyseal Fracture Trial

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorKolding Sygehus

About this trial

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.

Eligibility criteria

Qualifiers

Fracture types 12A-C (OTA/AO classification)

Treatment within 14 days from trauma

Age 18-64 years for SHAFT-Y and ≥65 years for SHAFT-E

Patients must understand the information given and be able to read and speak Danish, Swedish or Norwegian to complete the study paperwork

Disqualifiers

Inability to give informed consent

Undisplaced shaft fracture (less than a cortex-wide displacement in all radiographic plane)

Vascular injury in ipsilateral arm

Polytrauma (defined as a trauma with one or more concurrent fractures to the upper extremities or other trauma absolute indications for surgical intervention)

Trial design

Treatments tested in this trial

  • Surgical treatment
  • Non-surgical treatment

Treatment groups

287 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Kolding Sygehus

Lead sponsor

Copenhagen University Hospital, Hvidovre

Collaborator

Zealand University Hospital

Collaborator

Oslo University Hospital

Collaborator

Helse Stavanger HF

Collaborator

Sahlgrenska University Hospital

Collaborator

Uppsala University Hospital

Collaborator

Odense University Hospital

Collaborator

Hospital of Southern Jutland

Collaborator

Slagelse Hospital

Collaborator

Aalborg University Hospital

Collaborator

University Hospital, Umeå

Collaborator

Nordsjaellands Hospital

Collaborator

Holbaek Sygehus

Collaborator

Aarhus University Hospital

Collaborator

Copenhagen University Hospital at Herlev

Collaborator

University Hospital Bispebjerg and Frederiksberg

Collaborator

Viborg Regional Hospital

Collaborator

Karolinska University Hospital

Collaborator

Danderyd Hospital

Collaborator

Tampere University Hospital

Collaborator

Helsinki University Central Hospital

Collaborator