Assessment of the Risk of Contralateral Non Simultaneous Neck of Femur Fracture in the Elderly.

Clalit Health Services

Status: Unknown

Conditions: Neck of Femur Fracture

Treatments: Other: CAT scan (CT scan)

Study type: Interventional

Funder types: Other

Identifiers

NCT02577081

0163-15-MMC

Details and patient eligibility

About

Neck of femur fractures are common in the elderly and are the source of significant morbidity and mortality. This study is based on a new technique developed in Ben Gurion University, with which investigators are able to asses the structural 3 dimensional strength of a bone by applying a unique simulation on a CAT scan of the bone. The purpose of this study is to evaluate the risk of a contralateral neck of femur fracture after the first neck of femur fracture and to estimate the potential fracture characteristics.

Full description

Neck of femur fractures are common in the elderly and are the source of significant morbidity and mortality. literature shows that around 10 percent of those who fracture their femoral neck for the first time will later fracture their contralateral neck of femur and in most cases with the same fracture characteristics. This study is based on a new technique developed in Ben Gurion University, with which investigators are able to asses the structural 3 dimensional strength of a bone by applying a unique simulation on a CAT scan of the bone. The purpose of this study is to evaluate the risk of a contralateral neck of femur fracture after the first neck of femur fracture and to estimate the potential fracture characteristics.

Enrollment: 100 estimated patients

Sex: All

Ages: 70 to 90 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• 70-90 years old patients admitted to the orthopaedic department after neck of femur fracture.
• No contra lateral femur pathology.
• Consent for pelvis and femurs CAT scan.

Exclusion criteria

• Known pathology in other lower limbs joints in the body.
• History of previous fractures or operations in lower limbs.

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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100 participants in 1 patient group

CAT scan

Experimental group

Description:

A CAT scan will be done for all participants. The scan will include the pelvis and 2 femurs.

Treatment:

Other: CAT scan (CT scan)