OUTCOMES OF HIP ARTHROPLASTY USING A DEPUY PINNACLE GRIPTION CUP

OUTCOMES OF HIP ARTHROPLASTY USING A DEPUY PINNACLE GRIPTION CUP - Pinnacle Gription Registry

Status

Active, not recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000032711

Enrollment

300

Registered

2018-06-10

Start date

2018-09-19

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

Patients who are indicated for primary total hip replacement including the following disease. -Rheumatoid arthritis -Hip Osteoarthritis -Avascular necrosis of the femoral head -Fracture of the femoral head -Acampsia -Arthrodesia, Osteotomy, Post-operative of femoral head replacement

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: 1. Patients 20 years of age or older at the time of consent 2. Primary Total hip replacement for any indication in accordance with the Instruction for Use accompanying the implant 3. Signed informed patient consent form

Exclusion criteria

Exclusion criteria: None

Design outcomes

Primary

Measure	Time frame
Evaluate the clinical outcomes of a series of total hip replacements using the DePuy Pinnacle Gription cup	—

Countries

Japan

Contacts

Public ContactAiko Fujiki

Johnson & Johnson K.K. Medical Company Clinical Research

AFUJIKI1@its.jnj.com03-4411-6789

Outcome results