Clinical Trials Directory

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UnknownNCT05884918

Intraoperative Hypotension in High-risk Patients Undergoing Surgery

Risk Factors and Frequency of Intraoperative Hypotension in High-risk Patients Undergoing Surgery: A Multicenter Observational Prospective Study

Status
Unknown
Phase
Study type
Observational
Enrollment
2,000 (estimated)
Sponsor
Mazovia Regional Hospital in Siedlce · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The primary objective of this observational study is to investigate the risk factors for intraoperative hypotension and identify the underlying pathomechanisms leading to it, both during the period after general anesthesia induction and throughout its course. The main questions it aims to answer are: * how frequent is intraoperative hypotension * what are the underlying pathomechanism causing it The study is including patients who have been identified as having a high risk of perioperative complications (ASA3 or ASA4). Patients included in the study undergo advanced hemodynamic monitoring during the procedure. Anesthesia induction, maintenance, and termination are conducted by an anesthesiologist in accordance with current medical knowledge, and the planned experiment does not in any way influence the course of action. Investigators will analyse medical documentation, including the patient's medical history, anesthesia records, and hemodynamic parameter data obtained from the hemodynamic monitor (an Excel file containing comprehensive data related to specific cardiovascular parameters) to describe the incidence of intraoperative hypotension and answer key questions in accordance with the designed study protocol.

Conditions

Timeline

Start date
2023-03-02
Primary completion
2025-01-01
Completion
2025-01-31
First posted
2023-06-01
Last updated
2023-06-01

Locations

1 site across 1 country: Poland

Source: ClinicalTrials.gov record NCT05884918. Inclusion in this directory is not an endorsement.