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Hypotension Predictive Index Effect on Intraoperative Hypotension During Pancreatic Surgery.

NCT06097052 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 48

Last updated 2024-03-06

No results posted yet for this study

Summary

Intraoperative hypotension (IOH) is a sudden clinical phenomenon that occurs frequently during general anesthesia. Prevention of IOH has been linked to reduced postoperative organ damage and decreased incidence of perioperative complications. Oncological patients with reduced preoperative physiological reserves may be especially vulnerable to IOH deleterious effects, especially when exposed to prolonged surgical time increase, as it is the case for patients undergoing pancreatic surgery.

The investigators aim to study introduction of a new technology able to predict hypotensive events (Hypotension Predictive Index, HPI Acumen™) in terms of its effects on IOH occurrence and burden in patients undergoing pancreatic surgery. The investigators will enroll patients before and after the introduction of HPI monitoring. Further, differences in postoperative outcomes and perioperative complications between before and after populations will be investigated.

Conditions

  • Hypotension During Surgery
  • Perioperative Complication

Interventions

DEVICE

Hypotension Predictive Index

Introduction of Hypotension Predictive index and transition from a reactive to a proactive approach of intraoperative hypotension treatment.

Sponsors & Collaborators

  • Istituto Clinico Humanitas

    lead OTHER

Principal Investigators

  • Federico Piccioni · Istituto Clinico Humanitas

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-05-23
Primary Completion
2023-12-01
Completion
2024-01-31
FDA Device
Yes

Countries

  • Italy

Study Locations

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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 NCT06097052 on ClinicalTrials.gov