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comparision of different protamine to heparin dosing strategies in cardiac surgeries requiring cardio pulmonary bypass

Phase 1
Conditions
Health Condition 1: I20-I25- Ischemic heart diseases
Registration Number
CTRI/2021/02/031467
Lead Sponsor
Balabhadra Sai Priyanka
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

patients undergoing cardiac surgery requiring cardiopulmonary bypass

Exclusion Criteria

known defects of haemostatic system

thrombocytopenia

surgeries requiring dhca

patients who didnt stop clopidogrel 5 days prior to surgery

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
to compare ACT after 0.75:1 protamine to heparin ratio with 1:1 protamine to heparin ratioTimepoint: 1.BASELINE ACT at the start of surgery <br/ ><br>2.ACT after giving heparin 4mg/kg <br/ ><br>3.ACT immediately after reversal from protamine <br/ ><br>4.ACT after 30 min after reversal from protamine
Secondary Outcome Measures
NameTimeMethod
1.To study protamine adverse reactions. <br/ ><br>2.To compare peri-operative blood loss and utilization of blood products in both groups. <br/ ><br>3.To study effect of temperature on dose requirements of protamine. <br/ ><br>Timepoint: 1.Bleed from mediastinal drains will be quantified for 3 hours. <br/ ><br>2.Haemoglobin levels will be monitored for 3 hours. <br/ ><br>3.Coagulation profile after 4 hours of surgery. <br/ ><br>5.Transfusion requirements in first 48 hours after surgery <br/ ><br>
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