Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT04724811

Weight-bearing of Surgically Treated Acetabular Fractures.

Weight-bearing of Surgically Treated Acetabular Fractures. A Randomised Controlled Trial

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Hospital District of Helsinki and Uusimaa · Academic / Other
Sex
All
Age
60 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine whether patients with operatively treated acetabular fractures benefit from early weight-bearing as tolerated. The study compares two groups ( n = 25 each), which are randomised into either weight-bearing as tolerated or touch-down weight-bearing for 6-8 weeks postoperatively. Both study groups are stratified according to * Type of fracture (anterior approach vs anterior + additional posterior approach) * Dislocated dome vs non-dislocated/ non existing separate dome fragment Patients, who are eligible to participate in the trial but choose not to participate in randomisation are asked to enrol in a prospective cohort follow-up cohort. This is to examine a potential participation bias in the RCT groups. These patients will not be counted into the target amount of 50 RCT patients.

Detailed description

For the past 20 years, the established treatment of dislocated acetabular fractures has been surgical reduction and stable osteosynthesis. Good long-term results have been reported in these patients. At present, the mobilisation of these patients after surgery is generally restricted for several weeks ranging from 6-12 weeks touch-down- or non-weight-bearing with no uniform protocol. However there is no scientific evidence for limiting post operative weight-bearing. Accordingly the need of studies on weight-bearing surrounding periarticular fractures has been advocated. Acetabular fractures in the elderly population are becoming more common and pose significant challenges for treatment including postoperative rehabilitation. Our aim is to investigate if patients benefit of a more liberal weight-bearing regime postoperatively. The primary outcome is measured at 1 year, secondary outcomes are followed up to 10 years postoperatively

Conditions

Interventions

TypeNameDescription
PROCEDUREOpen reduction and internal fixation (ORIF)Approaches used: * Intrapelvic approach +/- iliac window * Kocher-Langenbeck approach

Timeline

Start date
2024-05-01
Primary completion
2026-12-01
Completion
2027-12-01
First posted
2021-01-26
Last updated
2024-03-06

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT04724811. Inclusion in this directory is not an endorsement.