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Polymethyl Methacrylate and (PEGT/PBT) Centralizer by the Uncemented BIHAPRO THP

NCT00214760 · Status: TERMINATED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 70

Last updated 2010-02-01

No results posted yet for this study

Summary

The purpose of this study is to analyse if the alignment of the stem and the number of complications of the new resorbable PEGT/PBT centralizer are comparable to the standard PMMA centralizer during the placement of an uncemented Bihapro hip prosthesis.

Conditions

Interventions

DEVICE

PGET

resolbable liner

DEVICE

PMMA

cement liner

Sponsors & Collaborators

  • Atrium Medical Center

    collaborator OTHER

  • Biomet Nederland BV

    lead INDUSTRY

Principal Investigators

  • Joanne Bloemsaat-Minekus, PhD · Biomet Nederland

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-05-31
Primary Completion
2008-08-31
Completion
2011-09-30

Countries

  • Netherlands

Study Locations

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Entities

Diseases

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 NCT00214760 on ClinicalTrials.gov