Total Hip Registry
1 other identifier
observational
942
1 country
1
Brief Summary
Objective 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Jul 2005
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
July 1, 2005
CompletedFirst Submitted
Initial submission to the registry
May 26, 2010
CompletedFirst Posted
Study publicly available on registry
May 28, 2010
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2018
CompletedStudy Completion
Last participant's last visit for all outcomes
December 1, 2018
CompletedJuly 26, 2016
July 1, 2016
13.4 years
May 26, 2010
July 22, 2016
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Harris Hip Score
2 weeks, 6 weeks, 3 months, 6 months, 1, 2, 5, 10 years
Study Arms (1)
Total hip
all consented patients receiving total hip arthroplasty
Eligibility Criteria
Population: All total hip replacements Selection: Males and non-pregnant females over the age of 21
You may qualify if:
- Patient requires total hip Arthroplasty
- Patient has signed IRB approved informed consent
You may not qualify if:
- Less than 21 years of age
- Patient is a prisoner
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Heekin Orthopedic Research Institutelead
- Stryker Orthopaedicscollaborator
- DePuy Orthopaedicscollaborator
- Restor3Dcollaborator
Study Sites (1)
Heekin Orthopedic Specialists
Jacksonville, Florida, 32204, United States
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Richard D Heekin, MD
Heekin Orthopedic Specialists
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- R. David Heekin, M.D.
Study Record Dates
First Submitted
May 26, 2010
First Posted
May 28, 2010
Study Start
July 1, 2005
Primary Completion
December 1, 2018
Study Completion
December 1, 2018
Last Updated
July 26, 2016
Record last verified: 2016-07