CompletedNot Applicable

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

Nepal80 participantsStarted 2019-07-23

Plain-language summary

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

Who can participate

SexALL

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

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

What they're measuring

ICU Length of Stay

Timeframe: 12 months

Trial details

NCT IDNCT07009730

SponsorTribhuvan University Teaching Hospital, Institute Of Medicine.

Sponsor typeOTHER

Study typeOBSERVATIONAL

Primary completion2020-07-22

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