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Study of role of wearable medical grade devices versus invasive monitoring in post operative cardiac surgery patients

A prospective observational study of role of wearable medical grade devices versus invasive monitoring in post operative cardiac surgery patients - NILL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2023/10/058594
Enrollment
85
Registered
2023-10-12
Start date
Unknown
Completion date
Unknown
Last updated
2025-03-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: I05- Rheumatic mitral valve diseases

Interventions

Intervention1: NIL: NIL Control Intervention1: NIL: NIL

Sponsors

AIIMS Rishikesh
Lead Sponsor

Eligibility

Inclusion criteria

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

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
1. Events of tachycardia 2. Events of brady cardia 3. events of bradypnoea 4. events of tachypnoea 5. events of atrial fibrillationTimepoint: 48 hrs—

Secondary

MeasureTime frame
To study the role of wearable devices in early detection of complicationsTimepoint: 48 hrs—

Countries

India

Contacts

Public ContactDr Anshuman Darbari

AIIMS RISHIKESH

darbarianshu@gmail.com9557511766

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026