- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05754905
High-resolution CE-MRA of Children's Hip Joint
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
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Chongqing
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Chongqing, Chongqing, China, 400014
- Children's Hospital of Chongqing Medical University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
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
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
Investigators
- Study Chair: Yuxi Su, M.D., Children's Hospital of Chongqing Medical University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
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)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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