Post Approval Study: NOVATION Ceramic Articulation Hip System

Stopped early · Not applicable

Conditions studied: Total Hip Replacement (Non-inflammatory)

In brief

The purpose of this study is to collect and evaluate long-term safety and effectiveness data on the Exactech® NOVATION ™ Ceramic Articulation Hip System ("NOVATION ™ Ceramic AHS").

Key facts

Study ID

NCT00715143

Run by

Exactech

People needed

126

Starts

2008-06-01

Expected to finish

2021-02-22

Last updated by the study team

2022-08-31

Who can join

Age: 21 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patient is undergoing primary hip surgery for symptomatic Non-inflammatory Degenerative Joint Disease (NIDJD). Composite diagnosis of NIDJD includes osteo/ degenerative arthritis, traumatic arthritis, congenital hip dysplasia and avascular necrosis.
• Patient is 21 years of age or older at the time of surgery.
• Patient is skeletally mature (tibial and femoral epiphyses are closed).
• Patient is willing and able to return for follow-up as specified by the study protocol over a ten (10) year post-operative follow-up period; including 5 years of in-clinic visits followed by 5 years of mail-in questionnaire follow-up.
• Patient is female and of childbearing age, for whom a negative urine pregnancy test is obtained immediately prior to surgery.
• Patient does not meet any of the Exclusion Criteria.
• Patient agrees to participate and sign the Informed Consent Form.

You may not qualify if…

• Patient will be less than 21 years old at the time of surgery.
• Patient is skeletally immature.
• Patient presents with inflammatory degenerative joint disease.
• Patient has evidence of active infection, but not including asymptomatic urinary tract infection (UTI) if treated with antibiotics preoperatively.
• Patient is female and of child bearing age and is pregnant or whose pregnancy status is unknown.
• Patient has neurological or musculoskeletal disease that may adversely affect gait or weight bearing.
• Patient has known presence of active metastatic or neoplastic disease (active is defined as within the past 5 years. Does not include basal cell carcinoma in cases when a subject with this diagnosis has undergone radical excision of the lesion, has pathological proof that the lesion has clean and clear peripheral and deep borders, and the location of the lesion is not near the operative hip or on the affected extremity).
• Patient has poor bone quality (e.g., osteoporosis) where, in the investigator's opinion, there is inadequate bone to support the implant(s).
• Patient has the presence of a previous prosthetic hip replacement device (any type, including THA, surface replacement arthroplasty, endoprosthesis, etc.) in the operative hip joint.
• Patient is known to have presence of a highly communicable disease or diseases that may limit follow-up (e.g., immuno-compromised conditions, hepatitis, active tuberculosis, etc.).
• Patient is a prisoner.
• Patient is obese where obesity is defined as a Body Mass Index (BMI) greater than 35. BMI = Weight (lbs.) ÷ Height (in.)2 x 703
• Patient has neuropathic joints.
• Patient has known allergies to the implant materials.
• Patient is unwilling or unable to comply with postoperative rehabilitation instructions and weight bearing limitations.
• Patient's life expectancy is < 5 years due to chronic diseases such as cancer, congestive heart failure, etc.
• Patient is unwilling or unable (e.g. cases of reduced mental capacity) to return for follow-up as specified by the study protocol over a ten (10) year post-operative follow-up period.
• Patient has reduced mental capability (permanent or temporary) that would prevent following pre-surgical and post-surgical instructions.
• Patient otherwise meets the study criteria but refuses to consent in writing to participate in the study.

Where it is running

• Shrock Orthopedic Research — Fort Lauderdale, Florida, United States
• Resurgens Orthopaedics — Cumming, Georgia, United States
• Fallon Clinic — Worcester, Massachusetts, United States
• Tulsa Bone & Joint Associates — Tulsa, Oklahoma, United States
• Hampton Roads Orthopaedics & Sports Medicine — Newport News, Virginia, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.