EMPHASYS Cup Position in THA With Non-Invasive Navigation (Velys Hip Navigation (VHN))
a study on Osteoarthritis Arthritis Rheumatoid Arthritis Dysplasia Avascular Necrosis of the Femoral Head Certain Cases of Ankylosis Hip Replacement
Summary
- Eligibility
- for people ages 21 years and up (full criteria)
- Location
- at UC Davis
- Dates
- study startedcompletion around
Description
Summary
The purpose of this research is to gather clinical and radiographic (X-ray) information about EMPHASYS™ acetabular shell (also called a hip 'cup') placement in total hip replacement surgery using a non-invasive surgical navigation system called VELYS™ hip navigation system with CUPTIMIZE™ Hip-Spine Analysis software.
Data collected in this study will be compared with data collected from implantations using different cup positioning instrumentation and techniques to assess performance.
Official Title
Planned vs. Actual Acetabular Cup Position in Total Hip Arthroplasty With Non-Invasive Navigation
Keywords
Osteoarthritis, Traumatic Arthritis, Rheumatoid Arthritis, Congential Hip Dysplasia, Avascular Necrosis of the Femoral Head, Certain Cases of Ankylosis, Arthritis, Hip Dislocation, Ankylosis, Necrosis, EMPHASYS Cup with VHN
Eligibility
You can join if…
Open to people ages 21 years and up
- All hip replacement component devices are to be used according to the approved indications.
- The subject is undergoing a standard of care primary uncemented hip replacement with the EMPHASYS cup and a CORAIL, EMPHASYS or ACTIS stem via the posterolateral, anterolateral, or direct lateral approach with the subject in the lateral decubitus position.
- The subject is a candidate for implantation utilizing the VELYS Hip Navigation system (and CUPTIMIZE pre-operative planning tool within the VELYS system).
- Individuals who are able to speak, read, and comprehend the Informed Consent Document and willing and able to provide informed subject consent for participation in the study and have authorized the transfer of his/her information to DePuy Synthes.
- Individuals who are willing and able to complete follow-up as specified by the study protocol.
- Individuals who are willing and able to complete the Subject Hip Outcomes questionnaires (i.e., FJS-12, EQ-5D-5L and Hip Evaluation) as specified by the study protocol.
- Individuals who are not bedridden per the discretion of the investigator.
- Individuals who are a minimum age of 21 years at the time of consent
You CAN'T join if...
- Active local or systemic infection.
- Loss of musculature, neuromuscular compromise or vascular deficiency in the affected limb rendering the procedure unjustified.
- Poor bone quality, such as osteoporosis, where, in the surgeon's opinion, there could be considerable migration of the prosthesis or a significant chance of fracture of the femoral shaft and/or the lack of adequate bone to support the implant(s).
- Charcot's or Paget's disease.
- The Subject is a woman who is pregnant or lactating.
- Subject had a contralateral amputation.
- Previous partial hip replacement in affected hip.
- Subject has participated in a clinical investigation with an investigational product (drug or device) in the last three months.
- Contralateral hip was replaced less than 6 months prior to surgery date.
- Subject is currently involved in any personal injury litigation, medical-legal or worker's compensation claims.
- Subject was diagnosed and is taking prescription medications to treat a muscular disorder that limits mobility due to severe stiffness and pain such as fibromyalgia or polymyalgia.
- Subject has a medical condition with less than 2 years of life expectancy.
- Subject, in the opinion of the Investigator, is a drug or alcohol abuser or has a psychological disorder that could affect their ability to complete subject reported questionnaires or be compliant with follow-up requirements.
Locations
- UC Davis Health System
Sacramento California 95817 United States - Florida Orthopaedic Institute
Gainesville Florida 32607 United States - CaroMont Hospital
Gastonia North Carolina 28054 United States
Details
- Status
- not yet accepting patients
- Start Date
- Completion Date
- (estimated)
- Sponsor
- DePuy Orthopaedics
- ID
- NCT06631638
- Study Type
- Interventional
- Participants
- Expecting 118 study participants
- Last Updated