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

Completed

• Conditions: Cardiac Surgery; Cardiac Surgery Requiring Cardiopulmonary Bypass

• Registration Number: NCT07009730
• Lead Sponsor: Tribhuvan University Teaching Hospital, Institute Of Medicine.

Brief Summary

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

Detailed Description

Not available

Study Timeline

• Study Start: 2019-07-23
• Primary Completion: 2020-07-22
• Study Completion: 2020-07-23
• Status Verified: 2025-05
• Study First Submitted: 2025-05-29
• Study First Submitted QC: 2025-06-06
• Last Update Submitted: 2025-06-06
• Study First Posted: 2025-06-08
• Last Update Posted: 2025-06-08

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 80

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

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
ICU Length of Stay	12 months	Measured in days from ICU admission to ICU discharge

Secondary Outcome Measures

Name	Time	Method
Duration of Cardiopulmonary Bypass (CPB)	12 months	Measured in minutes from initiation to termination of bypass

Trial Locations

Locations (1)

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