- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05112978
Evaluation of Patellar Dimension and Bristol Index in Asian Population
November 8, 2021 updated by: Ismail Hadisoebroto Dilogo, Indonesia University
Evaluation of Patellar Dimension and Bristol Index in Asian Population: an MRI Study
Restoration of patellar thickness is pivotal during a total knee arthroplasty (TKA).
Several studies showed there are differences in the knee measurements between Asian and Western population.
This study aims to evaluate the patellar dimension and Bristol Index of patellar width to thickness (BIPWiT) using magnetic resonance imaging (MRI) in Asian population.
Study Overview
Study Type
Observational
Enrollment (Actual)
101
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Jakarta, Indonesia
- Pondok Indah Hospital
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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
17 years to 40 years (Child, Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
all patients came to clinic
Description
Inclusion Criteria:
- knee pain
Exclusion Criteria:
- degenerative joint disease
- patellofemoral pathology
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: Other
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
bristol index
Time Frame: 1 day MRI examination
|
1 day MRI examination
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
patellar sizes
Time Frame: 1 day MRI examination
|
1 day MRI examination
|
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 (Actual)
January 1, 2019
Primary Completion (Actual)
December 31, 2020
Study Completion (Actual)
January 31, 2021
Study Registration Dates
First Submitted
November 2, 2021
First Submitted That Met QC Criteria
November 8, 2021
First Posted (Actual)
November 9, 2021
Study Record Updates
Last Update Posted (Actual)
November 9, 2021
Last Update Submitted That Met QC Criteria
November 8, 2021
Last Verified
November 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- BRIS
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
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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