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Control Mean Arterial Pressure in the Intensive Care Unit (COMAP-ICU)

Primary Purpose

Hypotension

Status
Completed
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
Automated adjustment of vasopressor
Manual adjustment of vasopressor
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypotension focused on measuring Intraoperative hypotension, intensive care unit, hemodynamic management

Eligibility Criteria

18 Years - 99 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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

Sites / Locations

  • Bicêtre Hospital
  • Paul Brousse Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Manual adjustment of vasopressor

Automated adjustment of vasopressor

Arm Description

Fluid and vasopressor will be managed as standard practice guided by the EV1000 monitoring device (manually infusion of both fluid and vasopressors) Objective being to maintain MAP within a target MAP range of 80-90 mmHg (fluid will be optimized and stroke volume index will be maintained within normal values)

Fluid will be managed using the EV1000 monitoring in order to optimize stroke volume index and vasopressor will be automatically deliver by a closed-loop system to maintain the MAP within the target range of 80-90 mmHg

Outcomes

Primary Outcome Measures

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)

Secondary Outcome Measures

Percentage of treatment time in hypertension (MAP > 90 mmHg)
Percentage of treatment time in hypertension (defined as a MAP > 90 mmHg)
Percentage of treatment time in hypotension (MAP < 80 mmHg)
Percentage of treatment time in hypotension (defined as a MAP < 80 mmHg)
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
Volume of fluid during the treatment time
Volume of fluid during the treatment time
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
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)

Full Information

First Posted
November 5, 2020
Last Updated
May 2, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
University of California, Irvine, University of California, Los Angeles, Erasme University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT04639037
Brief Title
Control Mean Arterial Pressure in the Intensive Care Unit
Acronym
COMAP-ICU
Official Title
Tight Postoperative Control of Mean Arterial Pressure Using a Closed-loop System for Norepinephrine Administration: A Randomized Controlled Trial in Patients Admitted to the Intensive Care Unit After a Major Surgery.
Study Type
Interventional

2. Study Status

Record Verification Date
April 2022
Overall Recruitment Status
Completed
Study Start Date
January 8, 2021 (Actual)
Primary Completion Date
January 26, 2022 (Actual)
Study Completion Date
January 26, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
Collaborators
University of California, Irvine, University of California, Los Angeles, Erasme University Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief 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.
Detailed 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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypotension
Keywords
Intraoperative hypotension, intensive care unit, hemodynamic management

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Active comparator (manual adjustment of vasopressor infusion) and Experimental (automated management of vasopressor infusion)
Masking
Participant
Allocation
Randomized
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Manual adjustment of vasopressor
Arm Type
Active Comparator
Arm Description
Fluid and vasopressor will be managed as standard practice guided by the EV1000 monitoring device (manually infusion of both fluid and vasopressors) Objective being to maintain MAP within a target MAP range of 80-90 mmHg (fluid will be optimized and stroke volume index will be maintained within normal values)
Arm Title
Automated adjustment of vasopressor
Arm Type
Experimental
Arm Description
Fluid will be managed using the EV1000 monitoring in order to optimize stroke volume index and vasopressor will be automatically deliver by a closed-loop system to maintain the MAP within the target range of 80-90 mmHg
Intervention Type
Device
Intervention Name(s)
Automated adjustment of vasopressor
Intervention Description
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)
Intervention Type
Device
Intervention Name(s)
Manual adjustment of vasopressor
Intervention Description
Fluid and vasopressor will be delivered as standard of care (manual adjustment of both fluid and vasopressor infusion rate by the nurse)
Primary Outcome Measure Information:
Title
Percentage of treatment time with a mean arterial pressure within 80-90 mmHg
Description
Percentage of treatment time in target (defined as a mean arterial pressure within 80-90 mmHg)
Time Frame
at DAY 0
Secondary Outcome Measure Information:
Title
Percentage of treatment time in hypertension (MAP > 90 mmHg)
Description
Percentage of treatment time in hypertension (defined as a MAP > 90 mmHg)
Time Frame
at DAY 0
Title
Percentage of treatment time in hypotension (MAP < 80 mmHg)
Description
Percentage of treatment time in hypotension (defined as a MAP < 80 mmHg)
Time Frame
at DAY 0
Title
Percentage of treatment time in hypotension (MAP < 65 mmHg)
Description
Percentage of treatment time in hypotension (defined as a MAP < 65 mmHg) which is the usual population target to correct
Time Frame
at DAY 0
Title
Volume of fluid during the treatment time
Description
Volume of fluid during the treatment time
Time Frame
at DAY 0
Title
Amount of vasopressor used during the treatment time
Description
total amount of vasopressor (norepinephrine) used during the treatment time to maintain MAP within 80-90 mmHg
Time Frame
at DAY 0
Title
Length of stay in the intensive care unit
Description
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)
Time Frame
up to 24 hours
Other Pre-specified Outcome Measures:
Title
mean Stroke volume index during the treatment time
Description
mean stroke volume index during the treatment time
Time Frame
at DAY 0
Title
mean Cardiax index during the treatment time
Description
mean cardiac index during the treatment time
Time Frame
at DAY 0

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
99 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Facility Information:
Facility Name
Bicêtre Hospital
City
Le Kremlin-Bicêtre
ZIP/Postal Code
94270
Country
France
Facility Name
Paul Brousse Hospital
City
Villejuif
ZIP/Postal Code
94800
Country
France

12. IPD Sharing Statement

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Control Mean Arterial Pressure in the Intensive Care Unit

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