Integrated intraoperative hemodynamic monitoring during cardiac surgery with CPB

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

HEMO-INTEGRA combines four intraoperative data streams—ventricular-arterial coupling, tissue perfusion and oxygen delivery, neuromonitoring, and venous congestion—into one dashboard. The study is observational and aims to assess feasibility and completeness of data capture at five perioperative timepoints, alongside standard monitoring. It is conducted at Clinica Medellin Sede Occidente in Medellín, Colombia, and does not alter clinical management or require additional procedures. Eligible participants are adults undergoing elective CPB surgery with standard TEE and arterial monitoring, with informed consent.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* \- Adult patients 18 years or older scheduled for elective cardiac surgery with cardiopulmonary bypass
* Standard intraoperative TEE and arterial line monitoring in place
* Written informed consent obtained

Exclusion Criteria:

* \- Emergency surgery
* Off-pump cardiac surgery (OPCAB)
* Inability to obtain adequate TEE window
* Refusal to participate

Where it's running

• Clinica Medellin Sede Occidente
  Medellín, Antioquia, Colombia Recruiting

Study contacts

• Principal investigator: Hernan D Castro-Arias, MD MSc — Clinica Medellin Sede Occidente, Grupo Quiron Salud
• Study coordinator: Hernan D Castro-Arias, MD MSc
• Email: hernan_castro@icloud.com
• Phone: +573128633884

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.