Safety and Effectiveness of the Hip Innovation Technology Reverse Hip Replacement System in Primary Total Hip Arthroplasty: A Pivotal Study

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Device
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this study is to determine if the use of the HIT Reverse Hip Replacement System is safe and effective in patients undergoing total hip replacement. We will determine whether it is safe and effective by comparing it to the control devices.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Maximum Age: 75
Healthy Volunteers: f
View:

• Patient requires primary THA due to NIDJD or any of its composite diagnoses such as osteoarthritis, avascular necrosis, posttraumatic arthritis, slipped capital epiphysis, fracture of the pelvis, and diastrophic variant requiring unilateral primary THA.

• Patient is between 50 (inclusive) and 75 (inclusive) years of age at the time of enrollment.

• Patient has preoperative medical clearance and is free from or treated for medical conditions that would pose excessive operative risk.

• Patient has a signed and dated Informed Consent Form (ICF).

• Patient is willing and able to participate in required follow-up visits at the investigational site and to complete study procedures and questionnaires.

Locations
United States
Florida
Miami Institute for Joint Reconstruction
RECRUITING
Miami
Advent Health Hospital, Carrollwood
RECRUITING
Tampa
Tampa General Health / Florida Orthopedic Institute
NOT_YET_RECRUITING
Tampa
Maryland
LifeBridge Health Rubin Institute for Advanced Orthopedics
RECRUITING
Baltimore
New Jersey
Division of Orthopaedic Surgery
RECRUITING
Somers Point
Ohio
JIS Orthopedics
RECRUITING
New Albany
Contact Information
Primary
George Diamantoni
g.diamantoni@hit-irh.com
1-866-832-4471
Time Frame
Start Date: 2022-07-15
Estimated Completion Date: 2035-07-15
Participants
Target number of participants: 288
Treatments
Experimental: Experimental Arm - HIT Reverse HRS
Subjects in the Experimental Arm will receive the HIT Reverse HRS Investigational Device. Implantation of the Investigational Device is performed using standard surgical procedures for THA, as described in the Instructions for Use (IFU). The control hip systems will be implanted in accordance with their respective IFU, which are also in line with standard surgical approaches for THA.
Active_comparator: Control Arm
Subjects in the Control Arm will receive one of the already-marketed semi- constrained uncemented hip systems using a metal-on-highly-cross-linked polyethylene (XLPE) or ceramic-on-XLPE bearing combination.
Sponsors
Leads: Hip Innovation Technology

This content was sourced from clinicaltrials.gov