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बा�� निलय �� शिथिलता वाल� र��िय�� म�� बिना पम�प �� सहायता �� दिल �� धमिनय�� �� शल�य �ि�ित�सा �� द�रान �म ��रा� म�� मिलर�न�न दवा �� निवार� भ�मि�ा

Pre-emptive role of low dose Milrinone infusion intra-operatively in patients with left ventricular dysfunction undergoing off-pump coronary artery bypass (OPCAB) surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2020/01/022851
Enrollment
60
Registered
2020-01-17
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: I251- Atherosclerotic heart disease of native coronary artery

Interventions

Intervention1: Milrinone: Dose: 0.375 microgram per kilogram body weight per minute Frequency: As continuous infusion through infusion Pump Route: Intravenous Duration: Intraoperative period, Immedia

Sponsors

GB pant institute of postgraduate medical education and research
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Adult patients posted for elective OPCAB 2. Adult patients with left ventricular dysfunction with ejection fraction less than or equal to 35%

Exclusion criteria

Exclusion criteria: 1. Patients having EF more than 35% 2. Patients simultaneously operated for any other surgery along with OPCAB 3. Patients having deranged renal functions 4. Patients having deranged hepatic function 5. Patients having thrombocytopenia or any known bleeding disorders 6. Patients having clinically significant arrhythmia 7. Patients having obstructive airway or lung parenchymal disease 8. Patients requiring dose of milrinone >0.5 μgm/kg/min 9. Patients requiring any other inotropic agents intraoperatively 10.Patients requiring conversion from OPCAB to ON PUMP CAB

Design outcomes

Primary

MeasureTime frame
Cardiac IndexTimepoint: Twenty minutes after starting infusion of drug/placebo followed by after every ten minutes of stabilizer application

Secondary

MeasureTime frame
systemic vascular resistance index, pulmonary venous resistance index, stroke volume indexTimepoint: Twenty minutes after starting infusion of drug/placebo followed by after every ten minutes of stabilizer application

Countries

India

Contacts

Public ContactDr Manish Kumar

GB pant institute of postgraduate medical education and research

akhleshtomar@gmail.com9718599403

Outcome results

None listed

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