A Study to Evaluate the Conformis Hip System

TerminatedOBSERVATIONAL
Enrollment

49

Participants

Timeline

Start Date

November 26, 2018

Primary Completion Date

June 6, 2022

Study Completion Date

June 6, 2022

Conditions
Clinical Condition Included in the Approved Indications For Use for the Conformis Hip System
Interventions
DEVICE

Conformis Hip System

The Conformis Hip System is an FDA cleared, uncemented, primary total hip replacement device composed of femoral and acetabular components. The system incorporates the use of a pre-operative CT scan to design patient-specific implants and instruments. Using patient imaging (CT scan), a patient-specific implant is designed that best meets the geometric and anatomic requirements of the specific patient. In addition, each Conformis Hip System device is shipped with an additional (optional) femoral stem (Cordera Femoral Stem).

Trial Locations (6)

25702

Scott Orthopedic Center, Huntington

33437

Personalized Orthopedic Research Institute, Boynton Beach

37203

Tennessee Orthopaedic Alliance, Nashville

80134

Denver Hip and Knee, Parker

89052

Orthopaedic Institute of Henderson, Henderson

95678

The Orthopedic Specialty Center of Northern California, Roseville

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Restor3D

INDUSTRY

NCT03738462 - A Study to Evaluate the Conformis Hip System | Biotech Hunter | Biotech Hunter