Clinical Outcomes Between Pulsatile and Non-Pulsatile Flow During Cardiopulmonary Bypass

Tribhuvan University Teaching Hospital, Institute Of Medicine.80 enrolled

Overview

The aim of this prospective, randomized study was to compare clinical outcomes of Pulsatile and non-pulsatile flow during Cardiopulmonary Bypass.

Study Type

OBSERVATIONAL

Enrollment

Conditions

Cardiac Surgery Cardiac Surgery Requiring Cardiopulmonary Bypass

Interventions

Bypassing AgentsPROCEDURE

Cardiopulmonary bypass surgery, pulsatile flow

Eligibility

Sex: ALL

Medical Language ↔ Plain English

Inclusion Criteria: * patients undergoing Atrial Septal Defect closure and Mitral Valve replacement Exclusion Criteria: * • Moderate and severe LVEF * • Patient with bleeding dysfunction;AKI ;deranged liver dysfunction\\ * • Patient/Surrogate decision maker not giving written informed consent

Locations (1)

Tribhuvan University Teaching Hospital, Institute of Medicine (IOM), Kathmandu, Nepal

Kathmandu, Nepal

Outcomes

Primary Outcomes

ICU Length of Stay

Measured in days from ICU admission to ICU discharge

Time frame: 12 months

Secondary Outcomes

Duration of Cardiopulmonary Bypass (CPB)

Measured in minutes from initiation to termination of bypass

Time frame: 12 months

Data from ClinicalTrials.gov

This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.