Experiment on the Use of Innovative Computer Vision Technologies for Analysis of Medical Images in the Moscow Healthcare System
1 other identifier
observational
133,000
1 country
1
Brief Summary
It is planned to integrate various services based on computer vision technologies for analysis of the certain type of x-ray study into Moscow Unified Radiological Information Service (hereinafter referred to as URIS). As a result of using computer vision-based services, it is expected:
- 1.Reducing the number of false negative and false positive diagnoses;
- 2.Reducing the time between conducting a study and obtaining a report by the referring physician;
- 3.Increasing the average number of radiology reports provided by a radiologist per shift.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Feb 2020
Longer than P75 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
February 21, 2020
CompletedFirst Submitted
Initial submission to the registry
July 17, 2020
CompletedFirst Posted
Study publicly available on registry
July 28, 2020
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2024
CompletedMay 26, 2023
May 1, 2023
3.9 years
July 17, 2020
May 25, 2023
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Number of errors
Change of at least 30% in the number of errors in interpretation of the studies with using computer vision-based services compared to the number of errors in interpretation without their application.
Upon completion, up to 4 years
Secondary Outcomes (3)
Report turnaround time
Upon completion, up to 3 year
Number of reports
Upon completion, up to 4 years
Change in the errors of services per the feedback form
Upon completion, up to 4 years
Study Arms (2)
Standard radiology studies with AI
The experiment is conducted on 10 types of studies with AI: 1. Chest CT/ LDCT with different pathologies; 2. Abdominal CT with different pathologies; 3. Head CT with different pathologies; 4. MSS XR with different fractures 5. Spine XR with different pathologies; 6. MMG; 7. Brain MRI with different pathologies; 8. Cervical spine MRI, Lumbosacral spine MR and Thoracic spine MRI with spine pathologies 9. Knee joint MRI 10. Lesser pelvis MRI.
Standard radiology studies without AI
The experiment is conducted on 10 types of studies without AI: 1. Chest CT/ LDCT with different pathologies; 2. Abdominal CT with different pathologies; 3. Head CT with different pathologies; 4. MSS XR with different fractures 5. Spine XR with different pathologies; 6. MMG; 7. Brain MRI with different pathologies; 8. Cervical spine MRI, Lumbosacral spine MR and Thoracic spine MRI with spine pathologies 9. Knee joint MRI 10. Lesser pelvis MRI.
Eligibility Criteria
patients over the age of 18 attending outpatient clinics
You may qualify if:
- Age (over 18 years)
- Gender (male and female)
- Referral for the study
- Signed informed consent to participate in the Experiment
- Chest computed tomography and Low-dose computed tomography for lung cancer detection or mammography for breast cancer detection or chest X-ray for lung pathology detection
You may not qualify if:
- Another type of study (including a different modality and anatomical area)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies of the Moscow Health Care Department
Moscow, Russia
Related Links
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Anton Vladzymyrskyy
Research and Practical Clinical Center for Diagnostics and Telemedicine Technologies of the Moscow Health Care Department
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- CASE CROSSOVER
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
July 17, 2020
First Posted
July 28, 2020
Study Start
February 21, 2020
Primary Completion
January 1, 2024
Study Completion
January 1, 2024
Last Updated
May 26, 2023
Record last verified: 2023-05
Data Sharing
- IPD Sharing
- Will not share