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Bone Remodeling Around a Trabecular Titanium Cup in Total Hip Arthroplasty

NCT06287021 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 50

Last updated 2025-09-02

No results posted yet for this study

Summary

The goal of this randomized controlled trial is to measure the periprosthetic bone mineral density changes around a 3D-printed highly-porous titanium acetabular cup used in primary total hip arthroplasty compared to a standard hydroxyapatite/titanium plasma-sprayed acetabular cup up to 2-year follow-up.

Conditions

  • Total Hip Arthroplasty

Interventions

DEVICE

Jump System Traser® cup

Press-fit, cementless, 3D-printed, highly-porous trabecular titanium acetabular cup

DEVICE

Jump System HAX-Pore® cup

Press-fit, cementless, hydroxyapatite/titanium plasma-sprayed acetabular cup

Sponsors & Collaborators

  • Permedica spa

    lead INDUSTRY

Principal Investigators

  • Lorenzo Banci, MSc · Permedica Orthopaedics, Merate, Italy

  • Giuseppe Peretti, MD · IRCCS Ospedale Galeazzi-Sant'Ambrogio, Milan, Italy

  • Paolo Sirtori, MD · Istituto Clinico San Siro, Milan, Italy

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-04-09
Primary Completion
2028-06-30
Completion
2028-06-30

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06287021 on ClinicalTrials.gov