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Vasopressin in cardiac surgery

Not Applicable
Conditions
Health Condition 1: I501- Left ventricular failure, unspecifiedHealth Condition 2: O- Medical and SurgicalHealth Condition 3: I978- Other intraoperative and postprocedural complications and disorders of the circulatory system, not elsewhere classified
Registration Number
CTRI/2022/12/048218
Lead Sponsor
Postgraduate Institute of Medical Education and Research
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Planned for elective cardiac surgery with CPB and presenting with LV dysfunction preoperatively.

LV dysfunction will be identified by the presence of LV EF < 50% on the last available preoperative echocardiography report, except in patients with severe mitral regurgitation where the cutoff for LV EF will be <60%.

Exclusion Criteria

Preoperative requirement of vasopressors/inotrope/mechanical circulatory support

Pregnancy

Patients undergoing simultaneous non cardiac surgery

Patients on renal replacement therapy

Patients with model for end-stage liver disease

Patients taking drugs for thyroid or adrenal disease

Documented peripheral vascular disease disease

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cardiac indexTimepoint: 30 minutes post cardiopulmonary bypass
Secondary Outcome Measures
NameTimeMethod
Heart rate, blood pressure, inotrope dose, blood gas investigations, cardiac index, left ventricle myocardial performance index, left ventricle systolic, diastolic functionTimepoint: Baseline, 30 minutes post CPB, and 0, 6, 12 and 24 hours in ICU;Hospital stay, MortalityTimepoint: 30 days post-operatively;Mechanical ventilation duration, ICU stay, Incidence of atrial fibrillation, requirement of renal replacement therapy, incidence of acute mesentric ischemia, peripheral cyanosisTimepoint: During ICU stay
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