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Clinical Trials in the Netherlands / NCT06367829
Enrolling by invitation Observational

Lubinus SPII Hip Stem Target Trial Emulation

NCT06367829 · tracked via the Priya Life Science Netherlands tracker
Phase
Observational
Started
2024-01-08
Last updated
2026-05-14

Condition(s) studied

Treatment Outcome

Investigational drug(s) / intervention(s)

Lubinus SPII hip stem 130mmLubinus SPII hip stem 150mm

Lubinus SPII hip stem 130mm: Shorter length of the SPII hip stem

Lubinus SPII hip stem 150mm: Longer length of the SPII hip stem

Study summary

The research questions this study aims to answer are as follows:

Primary research question:

"Do primary total hip arthroplasties for patients with OA, hip fracture or osteonecrosis with the 150mm Lubinus SPII hip stem have better mortality and stem revision rates than primary total hip arthroplasties with the 130mm hip stem?"

Secondary aims include:

* How does line-to-line cementation, compare to undersized cementation in primary total hip arthroplasty for patients with OA, hip fracture, or osteonecrosis when comparing equal size Lubinus SPII hip stems implanted with different cementation techniques?
* Does the Lubinus SPII 150mm hip stem perform equal to the Lubinus SPII 130mm hip stem in primary total hip arthroplasties for patients with OA, hip fracture or osteonecrosis when comparing patient reported outcome measures?

To answer these questions, this study has been allowed use of registered data from the LROI (dutch arthroplasty registry) and the SAR (swedish arthroplasty registry). After exclusion of patients who did not meet inclusion criteria between 2007-2020, approximately 110000 patients remain eligible for analysis.

Eligibility

Sex
ALL
Min age
5 Years
Max age
105 Years
Healthy volunteers
No
Inclusion Criteria: * Listed in registry for primary hip arthroplasty. * Listed in registry with an indication of osteoarthritis, osteonecrosis or hip fracture. * Received the Lubinus SPII hip stem, 130mm or 150mm, for their primary hip arthro- plasty. * End point listed in registry (Alive, Deceased or revision). Exclusion Criteria: * Patients who received the Lubinus SPII 150 XL conus stem.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
OLVG Amsterdam North Holland

More JointResearch trials in the Netherlands

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 NCT06367829 on ClinicalTrials.gov ↗ ← All trials in the Netherlands