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Clinical Evaluation of Vanguard DD RP

NCT04076202 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 113

Last updated 2024-05-17

No results posted yet for this study

Summary

This is a single cohort, prospective study of performance and safety of the Vanguard Deep Dish Rotating Platform (DD RP) cementless fixation with the goal to acquire clinical outcomes data and evaluate the performance of the device in an Austrian patient population

Conditions

Interventions

DEVICE

Cementless Vanguard DD RP

Patients treated with the Cementless Vanguard DD RP knee implant

Sponsors & Collaborators

  • Zimmer Biomet

    lead INDUSTRY

Principal Investigators

  • Sabine Illi, PhD · Clinical Evidence Manager

  • Tobias Gotterbarm, Prof. Dr. · Kepler Universitäts Klinikum

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-07-11
Primary Completion
2018-08-26
Completion
2026-12-31

Countries

  • Austria

Study Locations

More Related Trials

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 NCT04076202 on ClinicalTrials.gov