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Individualized Fluid And Vasopressor Administration In Surgical Patients

NCT03965793 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 38

Last updated 2021-03-02

No results posted yet for this study

Summary

The purpose of this study is to compare two different strategies of intraoperative mean arterial pressure (MAP) and stroke volume index management in high-risk patients undergoing major abdominal and orthopedic surgery (manual versus automated) The investigators hypothesis is that the automated group will spend less time during surgery in hypotension (defined as a MAP\<90% of patient's MAP baseline) compared to the manual group.

Conditions

  • Intraoperative Hypotension

Interventions

DEVICE

Automated management of hypotension

Fluid and vasopressor will be administered based on a novel automated clinical decision support system.

Sponsors & Collaborators

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Alexandre Joosten, MD PhD · Bicetre hospital, APHP.

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

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

Timeline & Regulatory

Start
2019-10-27
Primary Completion
2020-07-26
Completion
2020-07-26

Countries

  • France

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 NCT03965793 on ClinicalTrials.gov