NCT05186168Active, not recruiting
Corin MiniHip and Trinity Cup Clinical Surveillance Study
The Corin MiniHip and Trinity Advanced Bearing Acetabular Cup System UK Clinical Surveillance Study
Source: ClinicalTrials.gov · Last updated 1 Sept 2023
Brief summary (registry, in English)
The aim of the study is to provide long term follow up data on the performance and safety of the Corin MiniHip and Trinity acetabular cup over a 10-year period.
- Status (registry)
- Active, not recruiting
- Study type
- Observational
- Enrollment
- 546 (actual)
- First submitted
- 15 Dec 2021
- Start date
- 15 Mar 2011
- Primary completion date
- 3 May 2028
- Lead sponsor
- Corin
- Diseases
- Rheumatoid arthritis
- NCT number
- NCT05186168
What you commit to
- Study type: Observational
- Participants enrolled: 546
- From 15 Mar 2011 to the primary completion date, 3 May 2028
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Other illness
- Active infection
- Mental illness
- Distant foci of infections
- Metabolic disorders which may impair bone formation
- Muscular atrophy or neuromuscular disease
- Allergy to implant material
- Patients without sufficient quantities of synovial fluid to allow for proper lubrication, such as patients with Sjogren's syndrome
Other
- Severe Obesity (BMI over 35)
- Pregnancy
- Grossly distorted anatomy (surgeon's discretion)
- Sepsis
- Osteomyelitis
- Osteomalacia
- Osteoporosis
- Marked bone loss or bone resorption
- Skeletally immature patients and cases where there is a loss of abductor musculature, poor bone stock or poor skin coverage around the hip joint which would make the procedure inappropriate
- Any case not described in the inclusion criteria
- Any patient who cannot or will not provide informed consent for participation in the study
- Those whose prospects for a recovery to independent mobility would be compromised by known coexistent, medical problems.
Who the study is looking for
- A severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis or developmental dysplasia of the hip.
- Avascular necrosis of the femoral head
- All subjects must be between the age of 18 and 75 at the time of surgery to take part in this study
- Scheduled for a primary total hip replacement.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.