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Reducing Acute Kidney Injury Occurence by Administering Angiotensin II (AIDED)

Primary Purpose

Cardiac Surgery, Vasoplegia, Hyperreninemia

Status
Completed
Phase
Phase 3
Locations
Germany
Study Type
Interventional
Intervention
Angiotensin II
Control
Sponsored by
Westfälische Wilhelms-Universität Münster
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cardiac Surgery focused on measuring Cardiac Surgery, Acute kidney injury, Biomarker, Angiotensin II, Renin

Eligibility Criteria

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

Inclusion Criteria:

  • Adult patients undergoing cardiac surgery with CPB
  • Cardiac index 2.1l/min per square meter
  • Written informed consent
  • D-renin (difference between post- and preoperative) ≥ 3.7 micro Unit/ml 4 h after CPB
  • Postoperative hypotension requiring vasopressors

Exclusion Criteria:

  • Preexisting AKI (stage 1 and higher)
  • Patients with cardiac assist devices
  • Pregnant women, nursing women and women of childbearing potential
  • Known (Glomerulo-) Nephritis, interstitial nephritis or vasculitis
  • chronic kidney disease with estimated glomerular filtration rate (eGFR) < 30 ml/min
  • Dialysis dependent chronic kidney disease
  • Prior kidney transplant within the last to 12 months
  • Emergency surgery in the context of an acute coronary syndrome
  • Hypersensitivity to the active substance, or to any of the excipients of the study medication
  • Bronchospasm
  • Liver failure
  • Mesenteric ischemia
  • Participation in another intervention trial in the past 3 months
  • Persons with any kind of dependency on the investigator or employed by the institution responsible or investigator
  • Persons held in an institution by legal or official order

Sites / Locations

  • University Hospital Muenster

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Angiotensin II

Control

Arm Description

Intravenous infusion of max. 80 ng/kg/min Angiotensin II (titrated for each individual patient by effect) over 12 h after start of infusion

Intravenous infusion placebo (matched infusion volume) over 12 h after start of infusion

Outcomes

Primary Outcome Measures

• kidney damage after cardiac surgery identified by the difference between [TIMP-2]*[IGFBP7] levels 12h after randomization and [TIMP-2]*[IGFBP7] levels at randomization
The presence of tissue inhibitor of metalloproteinases (TIMP-2) and insulin-like growth-factor binding protein 7 (IGFBP7) in the urine will be measured.

Secondary Outcome Measures

Occurence of Acute Kidney Injury (AKI) according to the Kidney Disease: Improving Global Outcomes (KDIGO) criteria
Severity of Acute Kidney Injury
Number of patients with KDIGO stage 1, KDIGO stage 2 or KDIGO stage 3)
Amount of volume application
Fluid status
Dose of vasopressor use during intervention
Creatinine clearance on day one after cardiac surgery
Free-days through day 28 of vasoactive medications and mechanical ventilation
Renal Recovery
Renal recovery is defined as serum creatinine levels < 0.5 mg/dL higher than baseline serum creatinine
Mortality
Mortality
Mortality
Length of ICU (Intensive Care Unit) stay
Length of hospital stay
Use and duration of renal replacement therapy
Number of patients with renal replacement therapy
Major adverse kidney events (MAKE)
Major adverse kidney events consisting of mortality, dialysis dependency, persistent renal dysfunction (defined as serum creatinine ≥ 2x compared to baseline value)
Effect of Angiotensin converting enzyme inhibitor (ACEi)/angiotensin II receptor blocker (ARBs) use on the effect of angiotensin II
Correlation between the severity of hyperreninemia and the effect of angiotensin II

Full Information

First Posted
December 2, 2021
Last Updated
March 23, 2023
Sponsor
Westfälische Wilhelms-Universität Münster
Collaborators
German Research Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT05199493
Brief Title
Reducing Acute Kidney Injury Occurence by Administering Angiotensin II
Acronym
AIDED
Official Title
Biomarker-guided Implementation of Angiotensin-II (AT-II) to Reduce the Occurrence of Kidney Damage After Cardiac Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Completed
Study Start Date
December 27, 2021 (Actual)
Primary Completion Date
December 19, 2022 (Actual)
Study Completion Date
March 19, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Westfälische Wilhelms-Universität Münster
Collaborators
German Research Foundation

4. Oversight

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

5. Study Description

Brief Summary
The aim of this study is to evaluate whether adding angiotensin II to the standard of care is superior compared to the standard of care alone with respect to kidney damage (personalized approach) after cardiac surgery.
Detailed Description
Vasoplegic syndrome is a form of distributive shock that is characterized by low arterial pressure with reduced systemic vascular resistance and normal or elevated cardiac output that occurs in 5 to 25% of patients undergoing cardiac surgery. Patients with vasoplegic shock after cardiac surgery are at higher risk of organ failure, including acute kidney injury (AKI). Postsurgical AKI is associated with several adverse outcomes. Attempts to prevent AKI have largely been futile so far. Prior studies often started with the interventions after an AKI event, when a decline of kidney function (i.e. glomerular filtration rate) was already established. Application of norepinephrine is currently considered as the first-line therapy for vasoplegic shock, but all catecholamines have adverse effects, including myocardial ischemia and arrhythmias. In a recent observational trial, we demonstrated that there is a dysregulation in the renin-angiotensin-aldosterone system (RAAS) likely caused by a reduced angiotensin-converting enzyme (ACE) activity after cardiac surgery. Elevated renin levels identified patients at risk for AKI and were associated with cardiovascular instability and increased AKI rate after cardiac surgery. Furthermore, elevated renin levels could be used to identify high-risk patients for cardiovascular instability and AKI who would benefit from timely intervention with angiotensin II that could improve their outcomes. Therefore, the application of angiotensin II to treat a postoperative hypotension would mean a hormone substitution.Shock after cardiac surgery is associated with increased mortality. Cardiopulmonary bypass (CPB) represents a common clinical setting of sympathetic nervous system activation and cardiovascular instability. Vasoplegia is a form of distributive shock that is characterized by low arterial pressure with reduced systemic vascular resistance and normal or elevated cardiac output. It occurs in 5 to 25% of patients undergoing cardiac surgery. Patients with vasoplegia after cardiac surgery are at higher risk of organ failure, including AKI, and have an increased mortality rate and longer hospital length of stay. Clinical trials focusing on septic patients suggest that AT-II is a potent vasopressor. However, no human data exist whether the application of AT-II in cardiac surgery patients with y hyperreninemia high-risk patients identified by renin levels (individualized approach) reduces kidney damage and improves kidney function after cardiac surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiac Surgery, Vasoplegia, Hyperreninemia
Keywords
Cardiac Surgery, Acute kidney injury, Biomarker, Angiotensin II, Renin

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
64 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Angiotensin II
Arm Type
Experimental
Arm Description
Intravenous infusion of max. 80 ng/kg/min Angiotensin II (titrated for each individual patient by effect) over 12 h after start of infusion
Arm Title
Control
Arm Type
Placebo Comparator
Arm Description
Intravenous infusion placebo (matched infusion volume) over 12 h after start of infusion
Intervention Type
Drug
Intervention Name(s)
Angiotensin II
Intervention Description
Patients with Delta-renin >= 3.7 micro-unit/mL are at high risk for AKI. Patients who have a high delta-renin and a postoperative hypotension requiring vasopressors ad will be randomized. After randomization patients will receive intravenous infusion with the investigational drug.
Intervention Type
Drug
Intervention Name(s)
Control
Intervention Description
Patients with Delta-renin >= 3.7 micro-unit/mL are at high risk for AKI. Patients who have a high delta-renin and a postoperative hypotension requiring vasopressors ad will be randomized. After randomization patients will receive intravenous infusion with placebo
Primary Outcome Measure Information:
Title
• kidney damage after cardiac surgery identified by the difference between [TIMP-2]*[IGFBP7] levels 12h after randomization and [TIMP-2]*[IGFBP7] levels at randomization
Description
The presence of tissue inhibitor of metalloproteinases (TIMP-2) and insulin-like growth-factor binding protein 7 (IGFBP7) in the urine will be measured.
Time Frame
12 hours after start of intervention
Secondary Outcome Measure Information:
Title
Occurence of Acute Kidney Injury (AKI) according to the Kidney Disease: Improving Global Outcomes (KDIGO) criteria
Time Frame
72 hours after cardiac surgery
Title
Severity of Acute Kidney Injury
Description
Number of patients with KDIGO stage 1, KDIGO stage 2 or KDIGO stage 3)
Time Frame
72 hours after cardiac surgery
Title
Amount of volume application
Time Frame
12 hours after start of intervention
Title
Fluid status
Time Frame
12 hours after start of intervention
Title
Dose of vasopressor use during intervention
Time Frame
During intervention, an average of 12 hours
Title
Creatinine clearance on day one after cardiac surgery
Time Frame
One day after cardiac surgery
Title
Free-days through day 28 of vasoactive medications and mechanical ventilation
Time Frame
28 days after cardiac surgery
Title
Renal Recovery
Description
Renal recovery is defined as serum creatinine levels < 0.5 mg/dL higher than baseline serum creatinine
Time Frame
90 days after cardiac surgery
Title
Mortality
Time Frame
30 days after cardiac surgery
Title
Mortality
Time Frame
60 days after cardiac surgery
Title
Mortality
Time Frame
90 days after cardiac surgery
Title
Length of ICU (Intensive Care Unit) stay
Time Frame
up to 90 days after cardiac surgery (until discharge)
Title
Length of hospital stay
Time Frame
up to 90 days after cardiac surgery (until discharge)
Title
Use and duration of renal replacement therapy
Description
Number of patients with renal replacement therapy
Time Frame
up to 90 days after cardiac surgery
Title
Major adverse kidney events (MAKE)
Description
Major adverse kidney events consisting of mortality, dialysis dependency, persistent renal dysfunction (defined as serum creatinine ≥ 2x compared to baseline value)
Time Frame
90 days after cardiac surgery
Title
Effect of Angiotensin converting enzyme inhibitor (ACEi)/angiotensin II receptor blocker (ARBs) use on the effect of angiotensin II
Time Frame
12 hours after intervention
Title
Correlation between the severity of hyperreninemia and the effect of angiotensin II
Time Frame
12 hours after intervention

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adult patients undergoing cardiac surgery with CPB Cardiac index 2.1l/min per square meter Written informed consent D-renin (difference between post- and preoperative) ≥ 3.7 micro Unit/ml 4 h after CPB Postoperative hypotension requiring vasopressors Exclusion Criteria: Preexisting AKI (stage 1 and higher) Patients with cardiac assist devices Pregnant women, nursing women and women of childbearing potential Known (Glomerulo-) Nephritis, interstitial nephritis or vasculitis chronic kidney disease with estimated glomerular filtration rate (eGFR) < 30 ml/min Dialysis dependent chronic kidney disease Prior kidney transplant within the last to 12 months Emergency surgery in the context of an acute coronary syndrome Hypersensitivity to the active substance, or to any of the excipients of the study medication Bronchospasm Liver failure Mesenteric ischemia Participation in another intervention trial in the past 3 months Persons with any kind of dependency on the investigator or employed by the institution responsible or investigator Persons held in an institution by legal or official order
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alexander Zarbock, MD
Organizational Affiliation
University Hospital Muenster, Dept. of Anesthesiology, Intensive Care Medicine and Pain Therapy
Official's Role
Study Chair
Facility Information:
Facility Name
University Hospital Muenster
City
Münster
ZIP/Postal Code
48149
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No

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Reducing Acute Kidney Injury Occurence by Administering Angiotensin II

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