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Prospective Randomized Controlled Trial to compare Femoral neck shortening after two different treatment modalities

Prospective Randomized Controlled Trial to compare Femoral neck shortening after internal fixation of femoral neck fracture with sliding angular stable implant or multiple cannulated screws

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/12/038871
Enrollment
42
Registered
2021-12-23
Start date
Unknown
Completion date
Unknown
Last updated
2022-02-21

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

Conditions

Health Condition 1: V240- Motorcycle driver injured in collision with heavy transport vehicle or bus in nontraffic accident

Interventions

Intervention1: Group â?? FNS: Patients undergoing fixation with sliding angular stable implant with controlled collapse and Antirotation screw i.e. Femoral Neck System (FNS) Control Intervention1: Gro

Sponsors

nil
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria: o Patients having more than one fracture or any previous target or normal hip surgery o Prior target or normal hip arthritis o Smoker or tobacco chewer. o Patient having condition that preludes Co-operation and Compliance issues with rehabilitation in opinion of investigator

Design outcomes

Primary

MeasureTime frame
Primary objective To compare postoperative femoral neck shortening in between two groups and correlate it with patient reported outcome measures (PROMs)Timepoint: End of 11 months Completion of all cases At 14 months Completion of 3 monthly review of all cases End of 23 months Completion of final follow-up Within 2 years Data analysis, compilation and Submission of final report—

Secondary

MeasureTime frame
To compare clinical, functional and radiological outcomesTimepoint: 2 years—

Countries

India

Contacts

Public ContactSaurabh Gupta

AIIMS, Jodhpur

dr.saurabhortho@gmail.com7023578365

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026