Total Hip Registry

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details. Identifier: NCT01133249
Recruitment Status : Enrolling by invitation
First Posted : May 28, 2010
Last Update Posted : July 26, 2016
Stryker Orthopaedics
DePuy Orthopaedics
ConforMIS, Inc.
Information provided by (Responsible Party):
R. David Heekin, MD, Heekin Orthopedic Research Institute

Brief Summary:


Describe the clinical and demographic characteristics of patients who undergo hip arthroplasty and document post operative outcomes.

Examine the relationship between processes of care, hospital and surgeon associated outcomes

Provide expanded data to characterize existing and evolving practice patterns, delivery of care, and resource utilization in the management of knee arthroplasty patients.

Analyze and design ancillary studies to address unanswered questions.

Disseminate findings through publication in peer-reviewed scientific journals.

Condition or disease

Study Type : Observational
Estimated Enrollment : 942 participants
Observational Model: Cohort
Time Perspective: Prospective
Official Title: Total Hip Registry
Study Start Date : July 2005
Estimated Primary Completion Date : December 2018
Estimated Study Completion Date : December 2018

Resource links provided by the National Library of Medicine

U.S. FDA Resources

Total hip
all consented patients receiving total hip arthroplasty

Primary Outcome Measures :
  1. Harris Hip Score [ Time Frame: 2 weeks, 6 weeks, 3 months, 6 months, 1, 2, 5, 10 years ]

Information from the National Library of Medicine

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Ages Eligible for Study:   21 Years to 93 Years   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Population: All total hip replacements

Selection: Males and non-pregnant females over the age of 21


Inclusion Criteria:

  • Patient requires total hip Arthroplasty
  • Patient has signed IRB approved informed consent

Exclusion Criteria:

  • Less than 21 years of age
  • Patient is a prisoner

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its identifier (NCT number): NCT01133249

United States, Florida
Heekin Orthopedic Specialists
Jacksonville, Florida, United States, 32204
Sponsors and Collaborators
Heekin Orthopedic Research Institute
Stryker Orthopaedics
DePuy Orthopaedics
ConforMIS, Inc.
Principal Investigator: Richard D Heekin, MD Heekin Orthopedic Specialists

Responsible Party: R. David Heekin, MD, R. David Heekin, M.D., Heekin Orthopedic Research Institute Identifier: NCT01133249     History of Changes
Other Study ID Numbers: 05-09-01
First Posted: May 28, 2010    Key Record Dates
Last Update Posted: July 26, 2016
Last Verified: July 2016

Keywords provided by R. David Heekin, MD, Heekin Orthopedic Research Institute:
total hip

Additional relevant MeSH terms:
Joint Diseases
Musculoskeletal Diseases
Rheumatic Diseases