- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05548257
Mortality and Related Risk Factors After Hip Arthroplasty
September 16, 2022 updated by: RenJi Hospital
Mortality and Related Risk Factors After Hip Arthroplasty, a Retrospective Study
The patients who underwent hip arthroplasty in our hospital from January 2017 to December 2020 were reviewed.
The perioperative data were collected, and then the mortality was calculated and the risk factors were analyzed.
Study Overview
Status
Not yet recruiting
Study Type
Observational
Enrollment (Anticipated)
900
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Leilei WANG, master
- Phone Number: 8618801966298
- Email: wangleilei@renji.com
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
All adult patients undergoing hip arthroplasty in Renji Hospital.
Description
Inclusion Criteria:
- All patients undergoing hip arthroplasty in Renji Hospital during 2017.1-2020.12
Exclusion Criteria:
- Patients who did not undergo surgery after admission Age < 18 years Patients undergoing the second operation
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Observational Models: Case-Only
- Time Perspectives: Retrospective
Cohorts and Interventions
Group / Cohort |
---|
All patients were reviewed
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Risk factors of mortality one year after operation
Time Frame: From about even days before operation to 12 months after operation
|
From about even days before operation to 12 months after operation
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Risk factors of lower activities of daily living score at 12 months after operation
Time Frame: From about even days before operation to 12 months after operation
|
From about even days before operation to 12 months after operation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Anticipated)
September 20, 2022
Primary Completion (Anticipated)
August 4, 2023
Study Completion (Anticipated)
August 4, 2023
Study Registration Dates
First Submitted
September 16, 2022
First Submitted That Met QC Criteria
September 16, 2022
First Posted (Actual)
September 21, 2022
Study Record Updates
Last Update Posted (Actual)
September 21, 2022
Last Update Submitted That Met QC Criteria
September 16, 2022
Last Verified
September 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LY2022-012-B
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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