Study of role of wearable medical grade devices versus invasive monitoring in post operative cardiac surgery patients
Not Applicable
- Conditions
- Health Condition 1: I05- Rheumatic mitral valve diseases
- Registration Number
- CTRI/2023/10/058594
- Lead Sponsor
- AIIMS Rishikesh
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Patients above 18 years of age undergoing cardiac surgery (CABG/ valve/ congenital defects/ non-pump cardiac cases)
2. Informed consent for inclusion in the study.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Events of tachycardia <br/ ><br>2. Events of brady cardia <br/ ><br>3. events of bradypnoea <br/ ><br>4. events of tachypnoea <br/ ><br>5. events of atrial fibrillationTimepoint: 48 hrs
- Secondary Outcome Measures
Name Time Method To study the role of wearable devices in early detection of complicationsTimepoint: 48 hrs