Prospective Randomized Controlled Trial to compare Femoral neck shortening after two different treatment modalities
Not Applicable
- Conditions
- Health Condition 1: V240- Motorcycle driver injured in collision with heavy transport vehicle or bus in nontraffic accident
- Registration Number
- CTRI/2021/12/038871
- Lead Sponsor
- nil
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
All patients with displaced or non - displaced intra-capsular femoral neck fracture
No previous surgery of target or opposite hip
Patients who provide written informed consent
Patients must be eighteen years of age or older
Patients must be able to understand and follow instructions
Exclusion Criteria
oPatients having more than one fracture or any previous target or normal hip surgery
oPrior target or normal hip arthritis
oSmoker or tobacco chewer.
oPatient having condition that preludes Co-operation and Compliance issues with rehabilitation in opinion of investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Primary objective <br/ ><br>To compare postoperative femoral neck shortening in between two groups and correlate it with patient reported outcome measures (PROMs)Timepoint: End of 11 monthsCompletion of all cases <br/ ><br>At 14 monthsCompletion of 3 monthly review of all cases <br/ ><br>End of 23 monthsCompletion of final follow-up <br/ ><br>Within 2 yearsData analysis, compilation and Submission of final report <br/ ><br>
- Secondary Outcome Measures
Name Time Method To compare clinical, functional and radiological outcomesTimepoint: 2 years