A Prospective Clinical Study On A Total Hip Resurfacing System

N/ACompletedNCT00603395

St. Anna Ziekenhuis, Geldrop, Netherlands298 enrolled

Overview

This prospective clinical study is to demonstrate the efficacy and safety of ReCap Total Hip Resurfacing System.

Study Type

INTERVENTIONAL

Allocation

Purpose

TREATMENT

Masking

NONE

Enrollment

298

Conditions

Arthritis Avascular Necrosis

Interventions

ReCap Total Hip Resurfacing SystemDEVICE

This is a hip resurfacing system.

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * intended for skeletally mature individuals undergoing primary surgery as a result of hip degenerative joint disease, or any composite diagnoses, including: * Osteoarthritis * Avascular necrosis * Traumatic arthritis * Legg Perthes * Rheumatoid arthritis

Locations (1)

Knowledge Center for Orthopedic Surgery, St. Anna hospital

Geldrop, Netherlands

Outcomes

Primary Outcomes

Harris Hip Score, Device Revision/Removal, Radiographic Evaluation

Time frame: 2 years postoperative

Secondary Outcomes

Complications

Time frame: Anytime

Data from ClinicalTrials.gov

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