Clinical Trials in Sweden / NCT04350255
Recruiting
Not applicable
A Register Based Prospective Study During Implementation of a New Cup
NCT04350255 · tracked via the Priya Life Science Sweden tracker
Condition(s) studied
Prospective
Investigational drug(s) / intervention(s)
Total hip arthroplastyTotal hip arthroplasty
Total hip arthroplasty: Total hip arthroplasty with a Trident II hemispherical cup
Total hip arthroplasty: Total hip arthroplasty with a Trident II Tritanium cup
Study summary
In a prospective register-based study, we aim to evaluate the implant survival, clinical outcomes and X-ray findings by following a cohort of patients operated with the Trident II cup.
Eligibility
Inclusion Criteria:
* Primary hip replacement
* Eligible for uncemented fixation of the acetabular component
* Suitable for one of the stem designs from Stryker Orthopaedics
* Accepts follow-up according to the study protocol
Exclusion Criteria:
* Difficulties to understand written information due to language problems or other reasons
* Use of augments needed
* Acute hip fracture
* Tumor in the hip joint
Primary outcome measure(s)
- Implant survival at 3 years — 3 years
Kaplan Meier survival data, cup revision and risk of revision used as endpoints
Trial sites (1)
| Facility | City | Region | Status |
|---|---|---|---|
| Department of Orthopaedics | Mölndal | Västra Götaland County | Recruiting |
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Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04350255 on ClinicalTrials.gov ↗ ← All trials in Sweden