Wireless single lead ECG device for the detection of abnormal heart rhythms
Not Applicable
- Registration Number
- CTRI/2019/09/021260
- Lead Sponsor
- Sonia Mohandas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Arrythmia patients
Either gender
Willing to consent and wear the device continuously for 24-72 hours
Exclusion Criteria
Critically ill patients.
Participants who in the opinion of the investigator may not be co-operative or otherwise not eligible for the study.
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Heart rhythmTimepoint: After collecting, the data will be analysed within 2 days and report will be compared with standard holter device. Beats will be checked against normal sinus rhythm and abnormalities will be determined
- Secondary Outcome Measures
Name Time Method Heart rateTimepoint: Check whether the heart rates falls within normal range. greater than 60 beats per minute and less than 100 beats per minute.