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Femoral Neck System and Multiple Cannulated Screws in Femoral Neck Fracture

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Seoul National University

Status

Enrolling

Conditions

Femoral Neck Fractures

Treatments

Device: Femoral Neck System
Device: Multiple Cannulated Screw

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT04589598
FNS-MCS

Details and patient eligibility

About

Investigators will compare the clinical outcomes of femoral neck system with conventional multiple cannulated screw in non-displaced femoral neck fracture.

Full description

Clinical outcomes include reoperation, loss of fixation, and change of mobility.

Enrollment

620 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 18 years and older
  • non-displaced femoral neck fracture
  • community ambulator

Exclusion criteria

  • younger than 18 years
  • displaced femoral neck fracture
  • intertrochanteric fracture
  • subtrochanteric fracture

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

620 participants in 2 patient groups

FNS
Experimental group
Description:
those who are treated with femoral neck system (FNS)
Treatment:
Device: Femoral Neck System
MCS
Active Comparator group
Description:
those who are treated with multiple cannulated screw (MCS)
Treatment:
Device: Multiple Cannulated Screw

Trial contacts and locations

1

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Central trial contact

Young-Kyun Lee

Data sourced from clinicaltrials.gov

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