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Clinical Trials/CTRI/2024/02/062566
CTRI/2024/02/062566Not yet recruitingNot Applicable

Effect of the duration of Cardiopulmonary bypass on oxygenation predicted by measuring thoracic fluid content (TFC) using electrical cardiometry in infants undergoing closure of ventricular septal defect (VSD)

AIIMS1 site in 1 country30 target enrollmentStarted: March 1, 2024Last updated:

Trial Snapshot

Phase
Not Applicable
Status
Not yet recruiting
Sponsor
AIIMS
Enrollment
30
Locations
1
Primary Endpoint
To measure the change in Thoracic fluid content (TFC) using electrical cardiometry method with ICON monitor.

Study Overview

Brief Summary

For patients undergoing elective ventricular septal defect closure, the sensors of ICON monitor will be placed after induction and all Electrical Cardiometry parameters will be recorded along with blood gas analysis before and after coming off CPB

Study Design

Study Type
Observational

Eligibility Criteria

Ages
1.00 Month(s) to 1.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • infants between 1 month to 1 year, either sex, posted for elective surgical ventricular septal defect closure.

Exclusion Criteria

  • Parents who had not given consent, redo surgery, Palliative surgery, complex VSD, Infants with preoperative respiratory dysfunction, Infants with heart failure, difficulty in placing electrodes due to local site infection, and syndromic infants.

Outcomes

Primary Outcomes

To measure the change in Thoracic fluid content (TFC) using electrical cardiometry method with ICON monitor.

Time Frame: Before and After cardiopulmonary bypass.

Secondary Outcomes

  • To find a correlation between Thoracic fluid content (TFC) and its impact on oxygenation.(Before and After cardiopulmonary bypass.)

Investigators

Sponsor
AIIMS
Sponsor Class
Research institution and hospital
Responsible Party
Principal Investigator
Principal Investigator

Akshay Harikanth Laguduva

AIIMS

Study Sites (1)

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