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Cup Position in THA With Standard Instruments

NCT03189303 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 183

Last updated 2022-02-15

No results posted yet for this study

Summary

Prospective, global, multicenter study to assess cup position in THA. After written informed consent has been obtained, study evaluations will be collected from the pre-op clinic visit, the operative visit (including discharge), and 6 and 12 weeks postoperatively.

Conditions

  • Osteoarthritis; Rheumatoid Arthritis; Post Traumatic Arthritis

Interventions

DEVICE

Primary Uncemented Total Hip Arthroplasty

The study devices are the Pinnacle Hip System acetabular cup with a Summit, Actis, or Corail femoral stem

Sponsors & Collaborators

  • DePuy Orthopaedics

    lead INDUSTRY

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-09-07
Primary Completion
2021-05-19
Completion
2021-12-14
FDA Device
Yes

Countries

  • United States
  • Italy
  • Netherlands
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03189303 on ClinicalTrials.gov