Intraoperative Hypotension and Post-anesthesia Care Unit Recovery

NCT05671783 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 4776

Last updated 2023-01-20

No results posted yet for this study

Summary

The underlying causative mechanism that leads to intraoperative hypotension (IOH) may vary depending on the stage of anesthesia and surgery, which determines different IOH types. Naturally, the incidence and severity of IOH types will differ, as will the incidence and severity of postoperative complications.

Conditions

  • Post-induction Hypotension
  • Post Anesthesia Recovery
  • Hypotension
  • Intraoperative Hypotension

Interventions

OTHER

Hemodynamic observation of the patients.

For the purposes of this study, we defined intraoperative hypotension as a decrease in mean blood pressure of 30% from baseline for a minimum of 5 minutes, including induction and maintenance of anesthesia. The measuring blood pressure method (noninvasive or invasive) depended on the surgical intervention's invasiveness and the patient's cardiac performance. As soon as the patients entered the PACU, the responsible nurses started the standard monitoring. Anesthesiologists constantly oversee all actions based on the patient's condition. Clinical observation for respiratory and gastrointestinal problems and all disorders were monitored. When in room air SO2 was \<94, we started oxygen treatment with a 4 liter/minute nasal cannula, and in cases of nausea antiemetic was administered. The Modified Aldrete Score was used to discharge the patent.

Sponsors & Collaborators

  • Acibadem University

    lead OTHER

Principal Investigators

  • Lerzan Dogan, MD · Acibadem University

Eligibility

Min Age
18 Years
Max Age
85 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-05-06
Primary Completion
2022-11-30
Completion
2022-12-15

Countries

  • Turkey (Türkiye)

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05671783 on ClinicalTrials.gov