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The Warwick Hip Trauma Study

The Warwick Hip Trauma Study: a randomised clinical trial comparing interventions to improve outcomes in internally fixed intracapsular fractures of the proximal femur

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN49197425
Enrollment
225
Registered
2010-04-23
Start date
2009-08-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Topic: Musculoskeletal

Interventions

All participants will have a closed reduction of their fracture. The lower limb will be supported on a fracture table. Internal fixation of the fracture will be achieved through a standard lateral app

Sponsors

University of Warwick (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. All patients who present with intracapsular fractures of the proximal femur 2. Male and female, lower age limit of 65 years 3. With or without capacity to consent

Exclusion criteria

Exclusion criteria: 1. All patients who present late following their injury i.e. more than 48 hours after the index fracture 2. Patients with other serious injuries to either lower limb that would interfere with rehabilitation of the index fracture 3. Patients who are managed non-operatively 4. Patients younger than 65 years

Design outcomes

Primary

MeasureTime frame
The proportion of participants undergoing re-operation for failure of fixation within one year of sustaining the fracture.

Secondary

MeasureTime frame
1. Radiographic non-union rate at 12 months. Non-union will be defined as "failure of the fracture to show signs of bony union on the anteroposterior or lateral radiograph 1 year after surgery". 2. Radiographic evidence of failure of fixation at 6, 12 and 52 weeks 3. Radiographic evidence of avascular necrosis at one year 4. Magnetic resonance imaging at 6, 12 and 52 weeks. This measure will only be recorded for those participants with capacity to consent. 5. The EQ-5D score at 6, 12 and 52 weeks 6. Length of index hospital stay

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 31, 2026