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

Status

Unknown

Conditions

Intervention / Treatment

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

Study Contact Backup

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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