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Perioperative Personalized Blood Pressure Management

Primary Purpose

Blood Pressure, Intraoperative Hypotension, Postoperative Complications

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Personalized management
Sponsored by
Universitätsklinikum Hamburg-Eppendorf
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Blood Pressure focused on measuring Blood Pressure, Intraoperative Hypotension, Cardiovascular Dynamics

Eligibility Criteria

45 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age ≥ 45
  • American Society of Anesthesiologists physical status class (ASA) II-IV
  • scheduled for elective major surgery under general anesthesia
  • surgery expected to last ≥ 120 minutes

Exclusion Criteria:

  • emergency surgery
  • patients having liver or kidney transplantation
  • laparoscopic surgery
  • pregnancy
  • status of post transplantation of kidney, liver, heart, or lung
  • sepsis (according to current Sepsis-3 definition)
  • impossibility of preoperative automated blood pressure monitoring
  • MAP differences between the right and the left arm of more than 20 mmHg surgery that requires controlled hypotension

Sites / Locations

  • University Hospital RWTH Aachen
  • Department of Anesthesiology, Center of Anesthesiology and Intensive Care Medicine, University Medical Center Hamburg-Eppendorf

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

No Intervention

Arm Label

Personalized management group

Control group

Arm Description

Intraoperative MAP will be maintained at least at the mean nighttime MAP (assessed using preoperative automated blood pressure monitoring). If the mean nighttime MAP is below 65 mmHg, intraoperative MAP will be maintained at least at 65 mmHg.

Routine intraoperative blood pressure management with a lower intervention threshold of 65 mmHg. In contrast to the patients in the personalized management group, the individual mean nighttime MAP assessed using preoperative automated blood pressure monitoring is not taken into account and the treating anesthesiologists are blinded to the data of preoperative automated blood pressure monitoring.

Outcomes

Primary Outcome Measures

Individualized MAP target value
Difference between intraoperative target MAP (defined as the mean nighttime MAP assessed using preoperative automated blood pressure monitoring) and 65 mmHg; we consider a difference > ± 10 mmHg as clinically meaningful.

Secondary Outcome Measures

Proportion of patients with calculated MAP target
- proportion of patients in whom preoperative automated blood pressure monitoring + calculation of target MAP is possible
Duration and severity of MAP below MAP target
- time weighted average MAP below individual MAP target

Full Information

First Posted
April 24, 2021
Last Updated
February 27, 2023
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
RWTH Aachen University
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1. Study Identification

Unique Protocol Identification Number
NCT04894045
Brief Title
Perioperative Personalized Blood Pressure Management
Official Title
Perioperative Personalized Blood Pressure Management in Patients Having Major Surgery: a Bicentric Prospective Randomized Controlled Interventional Pilot Trial (IMPROVE-pilot)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Completed
Study Start Date
April 13, 2021 (Actual)
Primary Completion Date
November 24, 2022 (Actual)
Study Completion Date
November 27, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
RWTH Aachen University

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 investigators propose a pilot trial to (1) proof the concept that defining the intraoperative mean arterial pressure (MAP) intervention threshold based on the mean nighttime MAP (assessed using preoperative automated blood pressure monitoring) results in clinically relevant (mean nighttime MAP ± 10 mmHg) different target values compared with using an absolute population-derived MAP intervention threshold of 65 mmHg (primary endpoint); (2) investigate if a personalized perioperative blood pressure management is feasibly in multi-center studies, especially if the target values can be sufficiently achieved (secondary endpoint); (3) study the impact of personalized perioperative blood pressure management on the incidence of myocardial injury after non-cardiac surgery (MINS) (exploratory endpoint); (4) study the impact of personalized perioperative blood pressure management on the incidence of acute kidney injury within the first three postoperative days according to the KDIGO (Kidney Disease: Improving Global Outcomes) definition without oliguric criteria (exploratory endpoint).
Detailed Description
not provided

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Blood Pressure, Intraoperative Hypotension, Postoperative Complications
Keywords
Blood Pressure, Intraoperative Hypotension, Cardiovascular Dynamics

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Masking Description
In control group patients, the treating anesthesiologists are blinded to the data of preoperative automated blood pressure monitoring. Participants and outcomes assessors are blinded to group allocation.
Allocation
Randomized
Enrollment
105 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Personalized management group
Arm Type
Other
Arm Description
Intraoperative MAP will be maintained at least at the mean nighttime MAP (assessed using preoperative automated blood pressure monitoring). If the mean nighttime MAP is below 65 mmHg, intraoperative MAP will be maintained at least at 65 mmHg.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Routine intraoperative blood pressure management with a lower intervention threshold of 65 mmHg. In contrast to the patients in the personalized management group, the individual mean nighttime MAP assessed using preoperative automated blood pressure monitoring is not taken into account and the treating anesthesiologists are blinded to the data of preoperative automated blood pressure monitoring.
Intervention Type
Other
Intervention Name(s)
Personalized management
Intervention Description
Intraoperative MAP will be maintained at least at the mean nighttime MAP (assessed using preoperative automated blood pressure monitoring). If the mean nighttime MAP is below 65 mmHg, intraoperative MAP will be maintained at least at 65 mmHg.
Primary Outcome Measure Information:
Title
Individualized MAP target value
Description
Difference between intraoperative target MAP (defined as the mean nighttime MAP assessed using preoperative automated blood pressure monitoring) and 65 mmHg; we consider a difference > ± 10 mmHg as clinically meaningful.
Time Frame
1 day before surgery
Secondary Outcome Measure Information:
Title
Proportion of patients with calculated MAP target
Description
- proportion of patients in whom preoperative automated blood pressure monitoring + calculation of target MAP is possible
Time Frame
day of surgery
Title
Duration and severity of MAP below MAP target
Description
- time weighted average MAP below individual MAP target
Time Frame
day of surgery
Other Pre-specified Outcome Measures:
Title
Incidence of myocardial injury after non-cardiac surgery
Description
Incidence of myocardial injury after non-cardiac surgery assessed through measurement of baseline high-sensitivity troponin T (before surgery) and high-sensitivity troponin T on postoperative days 1,2, and 3.
Time Frame
baseline, postoperative days 1, 2 and 3
Title
Incidence of acute kidney injury
Description
Incidence of acute kidney injury within the first three postoperative days according to the KDIGO definition without oliguric criteria assessed through measurement of baseline creatinine (before surgery) and creatinine after surgery on postoperative days 1, 2, and 3.
Time Frame
baseline, postoperative day 1, 2 and 3

10. Eligibility

Sex
All
Minimum Age & Unit of Time
45 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age ≥ 45 American Society of Anesthesiologists physical status class (ASA) II-IV scheduled for elective major surgery under general anesthesia surgery expected to last ≥ 120 minutes Exclusion Criteria: emergency surgery patients having liver or kidney transplantation laparoscopic surgery pregnancy status of post transplantation of kidney, liver, heart, or lung sepsis (according to current Sepsis-3 definition) impossibility of preoperative automated blood pressure monitoring MAP differences between the right and the left arm of more than 20 mmHg surgery that requires controlled hypotension
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Bernd Saugel, Prof. Dr.
Organizational Affiliation
Department of Anesthesiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Karim Kouz, Dr.
Organizational Affiliation
Department of Anesthesiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital RWTH Aachen
City
Aachen
ZIP/Postal Code
52074
Country
Germany
Facility Name
Department of Anesthesiology, Center of Anesthesiology and Intensive Care Medicine, University Medical Center Hamburg-Eppendorf
City
Hamburg
ZIP/Postal Code
20246
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
27792044
Citation
Salmasi V, Maheshwari K, Yang D, Mascha EJ, Singh A, Sessler DI, Kurz A. Relationship between Intraoperative Hypotension, Defined by Either Reduction from Baseline or Absolute Thresholds, and Acute Kidney and Myocardial Injury after Noncardiac Surgery: A Retrospective Cohort Analysis. Anesthesiology. 2017 Jan;126(1):47-65. doi: 10.1097/ALN.0000000000001432.
Results Reference
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PubMed Identifier
30916004
Citation
Sessler DI, Bloomstone JA, Aronson S, Berry C, Gan TJ, Kellum JA, Plumb J, Mythen MG, Grocott MPW, Edwards MR, Miller TE; Perioperative Quality Initiative-3 workgroup; POQI chairs; Miller TE, Mythen MG, Grocott MP, Edwards MR; Physiology group; Preoperative blood pressure group; Intraoperative blood pressure group; Postoperative blood pressure group. Perioperative Quality Initiative consensus statement on intraoperative blood pressure, risk and outcomes for elective surgery. Br J Anaesth. 2019 May;122(5):563-574. doi: 10.1016/j.bja.2019.01.013. Epub 2019 Feb 27.
Results Reference
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Perioperative Personalized Blood Pressure Management

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