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Pinloc Versus Hansson Pins in the Treatment of Femoral Neck Fractures.

NCT02776631 · Status: UNKNOWN · Phase: NA · Type: INTERVENTIONAL · Enrollment: 537

Last updated 2019-04-17

No results posted yet for this study

Summary

A prospective randomized study comparing a new implant with three interlocked pins for internal fixation of femoral neck fractures (Hansson Pinloc System, Swemac Linköping, Sweden) versus 2 parallel pins with hooks (Hansson Pins, Swemac Linköping, Sweden).

Conditions

  • Femoral Neck Fractures

Interventions

DEVICE

Pinloc

Internal fixation device

DEVICE

Hansson Pins (LIH)

Internal fixation device

Sponsors & Collaborators

  • Sahlgrenska University Hospital

    collaborator OTHER

  • Department of Orthopedics, Motala

    collaborator UNKNOWN

  • Department of Orthopedics, Norrköping

    collaborator UNKNOWN

  • Department of Orthopedics, Nykoeping

    collaborator UNKNOWN

  • Department of Orthopedics, Eskilstuna

    collaborator UNKNOWN

  • Department of Orthopedics, Falun

    collaborator UNKNOWN

  • Department of Orthopedics, Uppsala University Hospital

    collaborator UNKNOWN

  • Department of Orthopedics, Helsingborg

    collaborator UNKNOWN

  • Torsten Johansson

    lead OTHER

Principal Investigators

  • Torsten Johansson, MD,Ass prof · Division of Orthopaedics, Department of Clinical and Experimental Medicine, Faculty of Health Sciences, Linköping University, Sweden.

  • Torsten Johansson, MD,Ass prof · Division of Orthopaedics, Department of Clinical and Experimental Medicine, Faculty of Health Sciences, Linköping University, Sweden.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-05-31
Primary Completion
2019-02-28
Completion
2019-12-31

Countries

  • Sweden

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02776631 on ClinicalTrials.gov