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Study identifier: NCT06748885 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Mpact 3D Metal Monolit Study

Condition: Total Hip Arthroplasty (THA)  ·  Sponsor: Medacta International SA

PhaseN/A
Planned participants88
Who can joinAll sexes, 18 Years to 75 Years
Healthy volunteersNo

About this study

Total hip arthroplasty (THA) is one of the most common operations performed in orthopaedics to improve a patient's quality of life. Surgeons are constantly seeking to improve all aspects of care related to this procedure, whether it be improving implant technology, improving instrumentation or the technique involved in performing the procedure. In recent years, a new porous titanium coating has been introduced to promote good osseointegration of uncemented cups. High friction torque and a feeling of immediate anchorage provide excellent primary stability, while high porosity ensures bone growth providing secondary stability. With higher porosity than standard coatings, a greater volume of bone can be present in the porous surface, giving a proportional increase in force at the interface. he Mpact 3D Metal Monolith cup has been designed to provide greater range of motion and improved joint stability, with a reduced risk of dislocation. It is an innovative design that improves stability and provides a favourable environment for long-term biological metal-bone fixation. The current study aims to collect clinical and radiological data to assess the function of the operated hip and the stability of the Mpact 3D Metal Monolith cup at 2 years and survival at 5 years for the treatment of patients requiring hip arthroplasty.

This description comes directly from the study's public registry record.

Talk to the study team

Philippe Anract  ·  01 58 41 30 38  ·  philippe.anract@aphp.fr

Always discuss trial participation with your own doctor first.

Locations (3)

Clinique BrétéchéNantes, FranceNot Yet Recruiting
Hôpital LariboisièreParis, FranceNot Yet Recruiting
Hôpital CochinParis, FranceRecruiting

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Source record: clinicaltrials.gov/study/NCT06748885