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Clinical study- Revelation® Hip System

Clinical study- Revelation® Hip System - Clinical study- Revelation® Hip System

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006107
Enrollment
100
Registered
2011-08-08
Start date
2011-09-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coxarthrosis

Interventions

Surgical technique (Anterolateral approach) Surgical technique(Posterior approach)

Sponsors

Shonan Kamakura Joint Reconstruction Center
Lead Sponsor
New York University Medical Center/Hospital for Joint Diseases
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who consent to treatment and are willing to provide informed consent 2) Patients not undergoing total hip arthroplasty (THA) 3) Patients are expected to cooperate with this study during the study period and are available for a minimum of 2 years clinical follow-up post surgical date.

Exclusion criteria

Exclusion criteria: 1) Patients undergoing joint replacement surgery or osteotomy at the affected limb. 2) Patients who have osteomyelitis at the proximal femur, hip suppurative infection and any other symptoms of infection. 3) Patients who have traumatic terminal osteoarthritis hip joint. 4) Patients who have a routine contraindication to surgery including but not limited to active infection, heart failure, lung failure or severe untreated bleeding abnormalities. 5) Pregnanancy 6) Mental impairment. 7) Patients under age 19 8) Metal allergy/ sensitivities 9) Others who the attending doctor decides not suitable for total hip arthroplasty and entry for this study.

Design outcomes

Primary

MeasureTime frame
Evaluation of statistical differences between the outcomes as a result of the different surgical approaches and technique.

Secondary

MeasureTime frame
Radiographic assessment: Diagnostic imaging assessment by bone density measurement, and clinical functional assessment.

Countries

Japan,North America

Contacts

Public ContactKoji Tsuji

Shonan Kamakura Joint Reconstruction Center Department of Orthopaedic Surgery

koji502@mac.com0467-47-2377

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026