A Post-Market Clinical Evaluation of the Treatment of Femur Fractures With the Femoral Nail GT

N/AActive Not RecruitingNCT04015128

Stryker Trauma and Extremities66 enrolled

Overview

This investigation is a prospective, multi-center clinical investigation. It is anticipated that a total of 50 subjects will be enrolled. Neither subjects nor investigators are blinded to treatment and the clinical investigation includes a historical control which will be compared to the Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System. Total duration of enrollment, 12 month follow-up and analysis is expected to take 25 months. The clinical investigation has been designed to follow the surgeon's standard of care for femur fractured subjects, in addition to a 12 month follow-up visit. The primary endpoint of this clinical investigation is to confirm efficacy/performance at 12 months, as measured by the Lower Extremity Measure (LEM). Confirmation of efficacy/performance at 12 months will be based on an equal or greater (non-inferior) LEM score result of the Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System compared to the T2 Femur benchmark literature.

The objective of this clinical investigation is to demonstrate the safety and efficacy/performance of the Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System. Efficacy/performance of the procedure will be measured by an equal or greater (non-inferior) Lower Extremity Measure (LEM) score result of the Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System compared to the T2 Femur benchmark literature at 12 months. In addition, demonstration of bone consolidation in correct alignment will be measured by Investigator assessment by 12 months. Safety of the Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System will be demonstrated through reporting of device related intra-operative and post-operative Adverse Events/incidents by 12 months.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Femoral Fracture

Interventions

Eligibility

Sex: ALLMin age: 18 YearsMax age: 80 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Subject is a male or non-pregnant female age 18 years or older at the time of surgery; * Subject is willing and able to give written informed consent and comply with the requirements of this Clinical Investigation Plan; * Subject is intended to be treated with the Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System in accordance with the following legally cleared/ approved Indications for Use: Indications for Use approved Outside of Europe include: * Fixation of subtrochanteric, intertrochanteric, ipsilateral neck/shaft, comminuted proximal femoral shaft fractures * Femoral fixation required as a result of pathological disease * Temporary stabilization of fractures of the femoral shaft ranging from the femoral neck to the supracondylar regions of the femur * Open and closed femoral fractures * Pseudoarthrosis and correction osteotomy * Pathologic fractures, impending pathologic fractures and tumor resections * Ipsilateral femur fractures * Fractures proximal to a total knee arthroplasty * Nonunions and malunions * Fractures involving osteopenic and osteoporotic bone Exclusion Criteria: * Subject is currently enrolled in or plans to enroll in any concurrent drug and/or device clinical investigation that, in the opinion of the Investigator, may confound results; * Per the Investigator, the subject is in poor general health or undergoing any concurrent disease that would place the subject in excessive risk to surgery (i.e. significant circulatory problems, cardiac disease).

Locations (6)

St. Cloud Orthopedic Associates, Ltd

Sartell, Minnesota, United States

Reno Orthopedic Clinic

Reno, Nevada, United States

NYU Langone Medical Center

New York, New York, United States

UC Health

Cincinnati, Ohio, United States

Regional One Health

Memphis, Tennessee, United States

Inova Fairfax Medical Campus

Falls Church, Virginia, United States

Outcomes

Primary Outcomes

Lower Extremity Measure (LEM)

The primary endpoint of this clinical investigation is to confirm efficacy/performance at 12 months, as measured by the Lower Extremity Measure (LEM). Confirmation of efficacy/performance at 12 months will be based on an equal or greater (non-inferior) LEM score result of the Femoral Nail GT of the T2 Alpha Femur Antegrade GT/PF Nailing System compared to the T2 Femur benchmark literature

Time frame: 12 months

Secondary Outcomes

Safety will be measured by capturing the incidence rate of device-related adverse events

Incidence of device-related adverse events will be monitored by 12 months through data collection and analyses.

Time frame: 12 months

Efficacy/Performance will be measured by demonstration of bone consolidation

Bone consolidation will be assessed by 12 months as measured by Investigator assessment.

Time frame: 12 months