Ireland
--:--IST
Latest
Clinical Trials in Sweden / NCT05657899
Recruiting Not applicable

The With Or Without Olecranon K-wires Trial

NCT05657899 · tracked via the Priya Life Science Sweden tracker
Phase
Not applicable
Started
2023-01-01
Last updated
2026-09-01

Condition(s) studied

Olecranon Fracture

Investigational drug(s) / intervention(s)

Cerclage fixationTension band wiring

Cerclage fixation: The intervention is by surgical open reduction and internal fixation of the fracture using two 1.0mm cerclage.

Tension band wiring: The intervention is by surgical open reduction and internal fixation of the fracture using a 1.0mm cerclage and two 1.6 mm k-wires as described in AO-guidelines.

Study summary

Fractures of the elbow tip (olecranon) that leave the elbow joint stable but where the fracture ends are separated (Mayo type 2a and 2b) can be treated with pins and a metal wire (tension band wiring, TBW) or metal wiring alone (cerclage fixation, CF ). Previous studies have reported high re-operation and complication rates following TBW. The current study's hypothesis, based on two retrospective studies, is that CF of these fractures yield lower re-operation rates compared with TBW. The investigators also hypothesize that the overall complication rate will be lower following CF. The aim is to investigate this hypothesis in a randomized controlled trial. Patients that are 18 years or older with Mayo type 2a and 2b olecranon fractures at Skåne University hospital will be invited to the study. Participation is voluntary. Patients who accept participation will be randomly assigned to surgery by either TBW or cerclage fixation. Two hundred participants will be followed by physiotherapists for 36 months post-surgery assessing re-operations, complications, patient reported outcome, and elbow function.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Sustained Olecranon type fracture of Mayo 2a or 2b * Seeking healthcare in at the Skåne University Hospital in Lund and Malmö, Sweden. Exclusion Criteria: * Subjects unable to participate in follow up (for example subjects with active substance abuse, dementia, inability to communicate or understand the questionnaires or subjects living in other administrative healthcare regions). * Subjects unable to give informed written consent. * Subject where non operative treatment is indicated due to frailty or severe ongoing disease. * Fracture not operated within 14 days from the date the fracture was sustained. * Subjects with severe open fractures of Gustilo-Anderson class III * Subject with pathological fractures from metastatic disease. * Subject with simultaneous or previous severe injury to the same arm are excluded for patient reported outcome measures but included for all other outcomes. * Subjects with previously severe injuries to the same arm will be excludes for PROM analyses but included for reoperation and complication analyses. * Subjects operated by an orthopedic trauma surgeons that did not attended our education on the study and the interventions, unless surgery is supervised by an orthopedic surgeon that has attended the education the subject will not be excluded.

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Dept. of Orthopaedics Lund Skåne County Recruiting
Dept. of Orthopaedics Malmö Skåne County Recruiting

More Region Skane trials in Sweden

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05657899 on ClinicalTrials.gov ↗ ← All trials in Sweden