Join us at Health Research Day — June 6th at Canton Waterfront Park, Baltimore!   Learn More →
← Back to all trials
Not Yet Recruiting NCT05784350

Preoperative Point of Care Ultrasound Guided Fluid Optimization and Intravenous Ondansetron to Prevent General Anesthesia-Induced Hypotension

Conditions: Intra-operative Hypotension

Sex: All
Ages: 19 Years – 99 Years
Healthy volunteers: No
Phase: NA
Enrollment: 150
Sponsor: Meir Medical Center

Location: Meir Medical Center Kfar Saba

Summary

Hypotension is a common side-effect of general anesthesia induction and is related to adverse outcomes including significantly increasing risk of one-year mortality. Even short durations of intraoperative hypotension have been associated with acute kidney injury (AKI) and myocardial injury.Half of all the patients were fluid-responsive, pointing to volume status as a significant risk factor. Ultrasound measurements of inferior vena cava (IVC) diameter with respiration, including the maximal diameter of the IVC (dIVCmax) at the end of expiration during spontaneous respiration and the collapsibility index (CI), have been recommended as rapid and noninvasive methods for estimating volume status. In attempt to prevent hypotension after spinal anesthesia induction, Ondansetron, a serotonin receptor antagonist, has been used effectively . Research Question Can preoperative IVC-US guided fluid optimization and intravenous ondansetron reduce the incidence of general anesthesia-induced hypotension in adult patients undergoing elective non-cardiac non-obstetric surgery?

Eligibility Criteria

Inclusion Criteria: 1. Age \> 18 2. Elective, non-cardiac, non-obstetric surgery under general anesthesia 3. American Society of Anesthesiologists physical status classification I - III Exclusion Criteria: 1. MAP below 60 mmhg prior to the induction of general anesthesia. 2. Patients treated with angiotensin converting enzyme inhibitors (ACE-I) or angiotensin receptor blockers (ARB) on the day of surgery. 3. Patients with heart failure with ejection fraction (EF) \< 40%. 4. Patients with documented acute or chronic renal failure. 5. Patients with hepatic failure. 6. Patients with neuraxial (spinal/epidural) anesthesia performed before induction of general anesthesia. 7. Patients with suspected difficult airway. 8. Patients with documented allergy to Ondansetron or prolonged QT-syndrome. \-

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT05784350). StuddyBuddy aggregates publicly available trial information.