Software for COVID19 Detection from Chest X-Ray, CT or Ultrasonography
Not Applicable
- Registration Number
- CTRI/2020/07/026351
- Lead Sponsor
- PurplAS IT Services Pvt Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
This study poses no additional health risk associated with standard Chest X-Ray, CT or Ultrasound procedures.
The medical information that will be collected from you if you take part in this study includes:
Your chest X-Ray, CT or Ultrasound Scan/Video.
You may be asked to take an RT-PCR or any other COVID19 confirmatory test.
Your Health data may be recorded for presence of any pre-existing diseases
Exclusion Criteria
Patients with conditions preventing them from undergoing standard chest X-Ray, CT or Ultrasound procedures.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The entire project aims to develop a market ready Artificial Intelligence based object recognition software capable of working on Real-time live Chest Radio-Imaging data like CT Scans, Ultrasound, and X-Ray as well as integrate the same with hardware prototype(s) capable of running the software.Timepoint: 2 Sub-phases: <br/ ><br>Data Collection & Testing: 4 weeks (Sensitivity Benchmarks will be outcome) <br/ ><br>Testing & Validation: 6 weeks (replication of Outcome/Sensitivity Benchmarks of week 4 over clinical scenario) <br/ ><br>
- Secondary Outcome Measures
Name Time Method Collection of Chest Radio-Imaging data like CT Scans, Ultrasound, and X-Ray from multiple COVID-19 patients and Refining of AI models for COVID19 detectionTimepoint: 4 weeks from start of trials;Test and validate sensitivity and reliability of COIVD19 identification in Controlled clinical scenarioTimepoint: 6 weeks from end of Secondary Outcome 1