None listed
Conditions
Interventions
None listed
Sponsors
PurplAS IT Services Pvt Ltd
Eligibility
Inclusion criteria
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
Exclusion criteria: Patients with conditions preventing them from undergoing standard chest X-Ray, CT or Ultrasound procedures.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 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: Data Collection & Testing: 4 weeks (Sensitivity Benchmarks will be outcome) Testing & Validation: 6 weeks (replication of Outcome/Sensitivity Benchmarks of week 4 over clinical scenario) | — |
Secondary
| Measure | Time frame |
|---|---|
| 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 | — |
Countries
India
Contacts
Public ContactAbhishek Biswas
PurplAS IT Services Pvt. Ltd.
Outcome results
None listed