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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04639037
Other study ID # APHP200709
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 8, 2021
Est. completion date January 26, 2022

Study information

Verified date April 2022
Source Assistance Publique - Hôpitaux de Paris
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this randomized controlled trial is to compare two different strategies of postoperative mean arterial pressure (MAP) management (manual versus automated) in patients who underwent a major surgery and admitted in the intensive care unit or post-anesthesia care unit for postoperative care. The investigators hypothesis is that the automated group will spend more time in a predetermined target MAP range of 80-90 mmHg compared to the manual group.


Description:

Although the correction of hypotension during the perioperative period should be a key goal, approximately 40% of overall mortality is still closely linked to the presence of perioperative hypotension which is responsible for significant morbidity particularly in patients undergoing major surgery. Indeed, inadequate management of perioperative hypotension remains an undeniable risk factor for morbidity and mortality. However, management of perioperative mean arterial pressure (MAP) is still suboptimal today. Indeed, the analysis of our database demonstrates that, on average, patient spends only 50-60 % of the treatment time within the predetermined MAP target. In about 10% of the treatment time, the patient is under-treated (hypotension) and 30% of the time, the patient is over-treated (hypertension). The correction of hypotension is achieved using vasopressor drugs (mainly norepinephrine infusion). In 2017 a study published in the JAMA shows that patients with tightly controlled arterial pressure have fewer organ dysfunctions than those with standard blood pressure management. However, maintaining MAP within a narrow range involves regular manual adjustments of norepinephrine infusion doses by intensive care unit nurses. When a hypotension occurs, there is usually two main possible treatments (fluid or vasopressors). In the operating room, for patients undergoing major surgery, we usually optimize fluid and vasopressor titration using an advanced hemodynamic monitoring device "EV1000 monitor" (Edwards Lifesciences, Irvine USA).This monitoring device can also be connected to a computer that controls a norepinephrine infusion pump in order to tightly adjust the infusion of norepinephrine to the target MAP predetermined by the clinician in charge of the patients. We have recently demonstrated that the use of such system resulted in less intraoperative time in hypotension compared to manual management. However, in the postoperative period, in patients admitted in the intensive care unit after a major surgery and requiring tight control of MAP, such demonstration is still lacking. Therefore, the objective of this randomized controlled superiority study is to demonstrate that, in patients admitted to intensive care unit or post-anesthesia care unit after a major surgery, tight control of MAP using a closed-loop system for vasopressor administration will result in MAP being more often within a predetermined MAP range of 80-90 mmHg compared to the same management without this automated closed-loop system (nurse adjustment of vasopressor administration).


Recruitment information / eligibility

Status Completed
Enrollment 53
Est. completion date January 26, 2022
Est. primary completion date January 26, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years to 99 Years
Eligibility Inclusion Criteria: - Adult Patients (>18 years) - Patients in the intensive care or post-anesthesia care unit after a major surgery and requiring norepinephrine infusion to maintain a MAP of 80-90 mmHg. - Patients equipped with an advanced hemodynamic monitoring device as standard of care during the surgery. - Patient with a social security number Exclusion Criteria: - Patients refusing to participate

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Automated adjustment of vasopressor
The objective of this randomized controlled superiority study is to demonstrate that, in patients admitted to intensive care after a major surgery, tight control of MAP using a closed-loop system for vasopressor administration will result in MAP being more often within a MAP range of 80-90 mmHg compared to the same management without this automated closed-loop system (nurse adjustment of vasopressor administration)
Manual adjustment of vasopressor
Fluid and vasopressor will be delivered as standard of care (manual adjustment of both fluid and vasopressor infusion rate by the nurse)

Locations

Country Name City State
France Bicêtre Hospital Le Kremlin-Bicêtre
France Paul Brousse Hospital Villejuif

Sponsors (4)

Lead Sponsor Collaborator
Assistance Publique - Hôpitaux de Paris Erasme University Hospital, University of California, Irvine, University of California, Los Angeles

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Other mean Stroke volume index during the treatment time mean stroke volume index during the treatment time at DAY 0
Other mean Cardiax index during the treatment time mean cardiac index during the treatment time at DAY 0
Primary Percentage of treatment time with a mean arterial pressure within 80-90 mmHg Percentage of treatment time in target (defined as a mean arterial pressure within 80-90 mmHg) at DAY 0
Secondary Percentage of treatment time in hypertension (MAP > 90 mmHg) Percentage of treatment time in hypertension (defined as a MAP > 90 mmHg) at DAY 0
Secondary Percentage of treatment time in hypotension (MAP < 80 mmHg) Percentage of treatment time in hypotension (defined as a MAP < 80 mmHg) at DAY 0
Secondary Percentage of treatment time in hypotension (MAP < 65 mmHg) Percentage of treatment time in hypotension (defined as a MAP < 65 mmHg) which is the usual population target to correct at DAY 0
Secondary Volume of fluid during the treatment time Volume of fluid during the treatment time at DAY 0
Secondary Amount of vasopressor used during the treatment time total amount of vasopressor (norepinephrine) used during the treatment time to maintain MAP within 80-90 mmHg at DAY 0
Secondary Length of stay in the intensive care unit length of stay in the intensive care unit (discharge at the discretion of the clinician in charge of the patient and not involved in the study protocol) up to 24 hours
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