A Prospective Clinical Study On A Total Hip Resurfacing System

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

Completed

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Key information

Conditions

Arthritis Avascular Necrosis Bone Diseases Joint Diseases Musculoskeletal Diseases Necrosis Osteonecrosis Pathologic Processes Pathological Conditions, Signs and Symptoms

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Knowledge Center for Orthopedic Surgery, St. Anna hospital

Geldrop, Netherlands

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

ReCap Total Hip Resurfacing System

Device

This is a hip resurfacing system.

Primary outcomes

Harris Hip Score, Device Revision/Removal, Radiographic Evaluation

Time frame: 2 years postoperative

Secondary outcomes

Complications

Time frame: Anytime

Sponsors and collaborators

Lead sponsor

St. Anna Ziekenhuis, Geldrop, Netherlands

Other

Registry information

Important dates

Study start: 2004
Primary completion: 2012
Study completion: 2014
First posted: Jan 29, 2008
Registry last updated: May 16, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.

Completed