- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05628792
In Vivo Depiction Of Bone Vascularization With UHR-CT CT And Deep Learning Algorithm Reconstruction: A Preliminary Study
November 23, 2022 updated by: GILLET Romain, Central Hospital, Nancy, France
To evaluate the image quality and ability to depict in vivo bone vascularization with an ultra-high-resolution computed tomography (UHR-CT) scanner using a deep learning reconstruction (DLR) and hybrid iterative reconstruction (HIR) algorithms, compared to simulated conventional CT, using osteoid osteoma (OO) as a model.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
20
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: romain gillet, MD
- Phone Number: 0680987216
- Email: romain_gillet3@hotmail.com
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 70 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
retrospective inclusion of all histologically proven Osteoid Osteoma referred to our department for CT imaging
Description
Inclusion Criteria:
- Proven osteoid osteoma
- Ultra High Resolution CT
Exclusion Criteria:
- None
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-Only
- Time Perspectives: Retrospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of cortical vessels
Time Frame: Retrospective review of all ultra high resolution CT of the precedent 2 years
|
Number
|
Retrospective review of all ultra high resolution CT of the precedent 2 years
|
|
Number of nidus vessels
Time Frame: Retrospective review of all ultra high resolution CT of the precedent 2 years
|
Number
|
Retrospective review of all ultra high resolution CT of the precedent 2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Confidence Score
Time Frame: Retrospective review of all ultra high resolution CT of the precedent 2 years
|
1 (weak) to 5 (strong)
|
Retrospective review of all ultra high resolution CT of the precedent 2 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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 (Anticipated)
December 20, 2022
Primary Completion (Anticipated)
January 31, 2023
Study Completion (Anticipated)
March 31, 2023
Study Registration Dates
First Submitted
October 28, 2022
First Submitted That Met QC Criteria
November 23, 2022
First Posted (Actual)
November 29, 2022
Study Record Updates
Last Update Posted (Actual)
November 29, 2022
Last Update Submitted That Met QC Criteria
November 23, 2022
Last Verified
November 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- N°2-RCB/EUDRACT
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.