CT Mar Technology and MR Mavric, Semac Sequence in Removing Artifacts of Orthopedic Metal Internal Fixation
Objective to Explore the Clinical Application Value of Spectral CT Mar Technology and Magnetic Resonance Mavric, Semac Sequence in Removing Artifacts of Orthopedic Metal Internal Fixation
1 other identifier
observational
50
1 country
1
Brief Summary
1\. Objective to compare the effect of single energy imaging and mar technology in reducing artifacts of knee and hip replacement, and to explore the appropriate keV range of Mar technology in removing metal artifacts.,2. Objective to compare the effects of different MRI sequences (mavric / semac, stir, ideal, FSE) in removing artifacts of spinal internal fixation, knee and hip replacement.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Dec 2019
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2019
CompletedStudy Completion
Last participant's last visit for all outcomes
October 30, 2020
CompletedFirst Submitted
Initial submission to the registry
June 29, 2021
CompletedFirst Posted
Study publicly available on registry
July 8, 2021
CompletedJuly 8, 2021
December 1, 2019
Same day
June 29, 2021
July 1, 2021
Conditions
Outcome Measures
Primary Outcomes (1)
Artifact index
AI in region of interest
2020.10.15-2020.10.30
Study Arms (2)
conventional examination
patients undergo conventional examination
Reduce metal artifacts examination
patients undergo reduce metal artifacts examination
Interventions
patients undergo reduce metal artifacts examination
Eligibility Criteria
From December 2019 to October 2020, patients who were reexamined after spinal internal fixation or knee and hip replacement in Peking University Third Hospital.
You may qualify if:
- Patients after spinal internal fixation or knee or hip replacement
You may not qualify if:
- Patients with poor image quality caused by their own factors such as patients' movement can not meet the diagnostic requirements
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Peking University Third Hospital
Beijing, Beijing Municipality, 010, China
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY CHAIR
Huishu Yuan
Peking University Third Hospital
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 29, 2021
First Posted
July 8, 2021
Study Start
December 1, 2019
Primary Completion
December 1, 2019
Study Completion
October 30, 2020
Last Updated
July 8, 2021
Record last verified: 2019-12