- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04182308
Anatomic Characteristics of Lisfranc Ligament in Vietnamese Adult
November 27, 2019 updated by: Nguyen Phu Chan, University of Medicine and Pharmacy at Ho Chi Minh City
Goal: the aim of this study is to determine the anatomic characteristic of lisfranc ligament
Study Overview
Detailed Description
Goal: the aim of this study is to determine the anatomic characteristic of lisfranc ligament, including components, thickness, height, and width, origins as well as relationship of center point of origin with neighbor structures in Vietnamese adults
Study Type
Observational
Enrollment (Anticipated)
30
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: Chan P Nguyen, doctor
- Phone Number: +84396722467
- Email: nguyenphuchan1993@gmail.com
Study Contact Backup
- Name: Phuc T Le, doctor
- Phone Number: +84974581490
- Email: ltphuc.nt18@ump.edu.vn
Study Locations
-
-
Ho Chi Minh
-
Ho Chi Minh City, Ho Chi Minh, Vietnam
- Recruiting
- Cho Ray Hospital
-
Contact:
- Hung P Do, professor
- Phone Number: +30123413
-
-
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 to 100 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
above ankle amputation samples at Cho Ray hospital, HCM city, Vietnam
Description
Inclusion Criteria:
- above ankle amputation samples at Cho Ray hospital, HCM city, Vietnam
Exclusion Criteria:
- foot injuries
- foot infection
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-Crossover
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Some anatomic characteristic of lisfranc ligament
Time Frame: 2 years
|
lenght, width
|
2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
relative position with neighbor structures
Time Frame: 2 years
|
cm
|
2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: Hung P Do, professor, Cho Ray Hospital
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
November 1, 2019
Primary Completion (Anticipated)
May 30, 2021
Study Completion (Anticipated)
July 30, 2021
Study Registration Dates
First Submitted
November 24, 2019
First Submitted That Met QC Criteria
November 27, 2019
First Posted (Actual)
December 2, 2019
Study Record Updates
Last Update Posted (Actual)
December 2, 2019
Last Update Submitted That Met QC Criteria
November 27, 2019
Last Verified
November 1, 2019
More Information
Terms related to this study
Other Study ID Numbers
- IRB00010195
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
IPD Plan Description
not yet
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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