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Testing efficacy of the point-of-care guided hemostatic management in cyanotic congenital cardiac surgery patients.

Not Applicable
Completed
Conditions
Health Condition 1: I52- Other heart disorders in diseasesclassified elsewhere
Registration Number
CTRI/2018/07/015122
Lead Sponsor
Department Of Science and Technology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
170
Inclusion Criteria

170 patients of either gender, belonging to ASA grade I â??

III undergoing elective cardiac surgery on CPB for cyanotic

congenital heart disease will be included in this study.

Exclusion Criteria

1. Patients on preoperative anticoagulants

2. Patients with known coagulopathy other than

inherent coagulopathy associated with cyanotic heart

disease.

3. Patients undergoing redo surgery

4. Patients undergoing cardiac surgery without

involving CPB will not be included in the study

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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