Testing a new system to improve care for people recovering from heart bypass surgery

An academic study of the effectiveness of enhancing post-operative care for CABG surgery through a novel patient monitoring and early warning system. - NIL

Status

Active, not recruiting

Phases

Phase 2Phase 3

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2024/01/061856

Enrollment

140

Registered

2024-01-25

Start date

Unknown

Completion date

Unknown

Last updated

2024-03-04

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

Conditions

Health Condition 1: O- Medical and Surgical

Interventions

Intervention1: Intervention: In the intervention arm of the study, in addition to all of the activities of the control arm (comparator) there will be a daily report on the physiological risk assessmen

Eligibility

Inclusion criteria

Inclusion criteria: 1.Patients who have undergone any of the following procedures: a. Isolated CABG, b.CABG+AVR, c.CABG+MVR or d. CABG+MV Repair 2.18-80 years of age at the time of admission

Exclusion criteria

Exclusion criteria: 1.Subjects who are known cases of HIV

Design outcomes

Primary

Measure	Time frame
Accuracy of identifying post-op complications earlier in the intervention arm >20% than control arm Timepoint: Post-operative Day 1 Post-operative Day 2 Post-operative Day 3	—

Secondary

Measure	Time frame
Optimise post-op patient workflow during the in-patient stayTimepoint: Post-operative days 1-7	—

Countries

India

Contacts

Public ContactDr Anusha Rohit

The Madras Medical Mission Hospital

anusha3rohit@gmail.com7299061739

Outcome results

None listed

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