High-resolution CE-MRA of Children's Hip Joint

March 3, 2023 updated by: Yuxi Su, Children's Hospital of Chongqing Medical University

High-resolution Contrast-enhanced Magnetic Mesonance Angiography of Children's Hip Joint

The goal of this observational study is to learn about the feasibility of enhanced three-dimensional water-selective cartilage (3D-WATSc) sequence in displaying the vessels of children's hip by magnetic resonance. The main questions it aims to answer are:

  • Could the images of enhanced 3D-WATSc sequence show the healthy side hip joint vessels in children?
  • Could the images of enhanced 3D-WATSc sequence show the vascular disease of the suffering side hip joint in children?

Participants with unilateral hip disease will undergo the magnetic resonance examination including enhanced 3D-WATSc sequence. The pelvic plain film and magnetic resonance images will be collected and analysed.

Researchers will compare the images of of the normal side with the images of the abnormal side to see if the enhanced 3D-WATSc sequence images could show the vascular disease of the suffering side hip joint in children?

Study Overview

Study Type

Observational

Enrollment (Actual)

48

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

    • Chongqing
      • Chongqing, Chongqing, China, 400014
        • Children's Hospital of Chongqing Medical University

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

6 months to 14 years (Child)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Children with hip disease from 2021-2022 in Children's Hospital of Chongqing Medical University

Description

Inclusion Criteria:

  • Children aged 6 months-14 years who are diagnosed as hip disease after screening by pediatric orthopedic surgeon in Children's Hospital of Chongqing Medical University during the study period. The hip disease contain developmental dysplasia of the hip, Perthes disease, infection of the hip, inflammation of the hip, fracture of the hip, and Meyer's dysplasia.

Exclusion Criteria:

  • patients with bilateral hip joint disease; patients with claustrophobia;Patients with metal implants (such as pacemaker implantation)

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

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Normal hip joint
The normal side of patients with hip joint disease
the two groups are underwent magnetic resonance examination including enhanced 3D-WATSc sequence
Abnormal hip joint
The abnormal side of patients with hip joint disease
the two groups are underwent magnetic resonance examination including enhanced 3D-WATSc sequence

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
The medial circumflex femoral artery (MCFA) and lateral circumflex femoral artery (LCFA) of the bilateral hip joint
Time Frame: 1 day (Magnetic resonance examination end time)
Morphology of the MCFA and LCFA of the bilateral hip joint
1 day (Magnetic resonance examination end time)
The branches of the MCFA and/or LCFA around the bilateral femoral neck
Time Frame: 1 day (Magnetic resonance examination end time)
Morphology of MCFA and/or LCFA branches around the bilateral femoral neck
1 day (Magnetic resonance examination end time)
The vessels of secondary ossification center and/or cartilaginous vascular canal in bilateral femoral head
Time Frame: 1 day (Magnetic resonance examination end time)
Morphology of the vessels and cartilaginous vascular canal in bilateral femoral head
1 day (Magnetic resonance examination end time)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Study Chair: Yuxi Su, M.D., Children's Hospital of Chongqing Medical University

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, 2021

Primary Completion (Actual)

December 30, 2022

Study Completion (Actual)

January 31, 2023

Study Registration Dates

First Submitted

February 23, 2023

First Submitted That Met QC Criteria

March 3, 2023

First Posted (Estimate)

March 6, 2023

Study Record Updates

Last Update Posted (Estimate)

March 6, 2023

Last Update Submitted That Met QC Criteria

March 3, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • CQMU-2023-2

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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