A Prospective Clinical Study On A Total Hip Resurfacing System

St. Anna Ziekenhuis, Geldrop, Netherlands

Status: Completed

Conditions: Arthritis; Avascular Necrosis

Treatments: Device: ReCap Total Hip Resurfacing System

Study type: Interventional

Funder types: Other

Identifiers

NCT00603395

EU-6

Details and patient eligibility

About

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

Enrollment: 298 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

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

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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298 participants in 1 patient group

ReCap

Other group

Description:

ReCap Total Hip Resurfacing System

Treatment:

Device: ReCap Total Hip Resurfacing System