A study where ultrasound images are collected and analysed to improve the speed and ease of use of ultrasound scanning on human beings
- Conditions
- Health Condition 1: null- Any indication for an ultrasound scanHealth Condition 2: Z000- Encounter for general adult medical examination
- Registration Number
- CTRI/2018/04/013418
- Lead Sponsor
- Philips India Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 250
1)Any subject presenting to the hospital/radiology unit for an imaging ultrasound scanner that will be performed on a Philips ultrasound.
2)100 Obstetric scans (from first, second and third trimesters of pregnancy)
3)About 10 cases in each of the other categories including cardiac, vascular, lung, musculoskeletal, abdominal, pelvic, breast, head and neck, paediatric (brain, abdomen), contrast and interventional ultrasound, etc. (150 total).
4)Adult patients must be willing and able to provide informed consent
5)Minors must provide assent (when possible) and also have concurrent parental permission
1)Subjects presenting with any condition that needs emergency care (as per investigatorâ??s discretion).
2)Adult patients unwilling or unable to provide informed consent
3)Minors unwilling to assent
4)Lack of parental permission of the minors
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method This is a data collection study, there are no specific primary clinical outcome other than collecting the ultrasound data as per clinical <br/ ><br>protocol. The primary endpoint of the study will be reached when <br/ ><br>250 subjects with data validated by the Sponsor have been enrolled. <br/ ><br>Time point: 250 subjects have been enrolled <br/ ><br>Timepoint: 250 subject enrollment in six months. End date 24th October 2018
- Secondary Outcome Measures
Name Time Method oneTimepoint: 6 months