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Recruiting NCT07022210

NCT07022210 Incidence of Hypotension in the Post-anesthesia Care Unit (PACU).

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Clinical Trial Summary
NCT ID NCT07022210
Status Recruiting
Phase
Sponsor Tomas Bata Hospital, Czech Republic
Condition Hypotension During Surgery
Study Type OBSERVATIONAL
Enrollment 100 participants
Start Date 2025-06-15
Primary Completion 2026-05-01

Trial Parameters

Condition Hypotension During Surgery
Sponsor Tomas Bata Hospital, Czech Republic
Study Type OBSERVATIONAL
Phase N/A
Enrollment 100
Sex ALL
Min Age 18 Years
Max Age 105 Years
Start Date 2025-06-15
Completion 2026-05-01

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Brief Summary

The perioperative period poses a heightened risk of complications for patients, including hypotension. While the issue of intraoperative hypotension is well-documented in medical literature, the occurrence and causes of hypotension in the post-anesthesia care unit often receive less attention. This phase of postoperative care, however, is vital for ensuring patient stability and preventing severe consequences. Failure to identify and manage a drop in blood pressure can lead to hypoperfusion of critical organs, increasing the risk of morbidity and mortality. The aim of this study is to examine the frequency of hypotension in the post-anesthesia care unit-defined as systolic blood pressure \<90 mmHg or a drop of more than 20% from baseline-and to identify factors contributing to its development.

Eligibility Criteria

Inclusion Criteria: * patients over 18 years old * patients undergoing a procedure under general anesthesia * patients who have consented to data processing * postoperative stay in PACU Exclusion Criteria: * patients younger than 18 years old. * patients transferred directly to the ICU/Anesthesiology and Resuscitation Department after surgery without staying in the recovery room. * patients with incomplete medical documentation or missing blood pressure values in the recovery room. * patients with a pre-existing diagnosis of resistant hypotension or unstable hemodynamics before surgery * patients with a history of long-term use of anxiolytics, antipsychotics, or other psychotropic medications that may affect cognitive function, emotional state, or predictive outcomes * patient refusal to participate in the study (including cases where they initially consented), with an emphasis on respecting patient autonomy

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