Vasopressin or Norepinephrine in Vasoplegic Shock After Non-cardiac Surgery (VANCSIII)
Primary Purpose
Circulatory Shock, Non-cardiac Surgery
Status
Withdrawn
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
Vasopressin
Norepinephrine
Sponsored by
About this trial
This is an interventional treatment trial for Circulatory Shock focused on measuring Vasopressin, Norepinephrine, Post-operative, Critical Care
Eligibility Criteria
Inclusion Criteria:
- Age greater than 18 years;
- Patients undergoing high-risk non-cardiac surgery;
- vasopressor need within 24 hours after surgery, defined as mean arterial pressure (MAP) <65 mmHg after volume resuscitation with at least 1 liter of crystalloid solution (Ringer's lactate) and maintaining a cardiac index> 2.2 ml / min / m²;
- Signature of the informed consent form.
Exclusion Criteria:
- Allergy to vasoactive drugs;
- Previous use of vasopressor;
- Gestation;
- Presence of Raynaud's phenomenon, altered Allen's test, systemic sclerosis or vasospastic diathesis;
- Severe hyponatremia (Na <130 mEq / L);
- Acute mesenteric ischemia;
- Acute coronary syndrome;
- Participation in another study;
- Refusal to participate in the study.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
Vasopressin group
Norepinephrine group
Arm Description
Blinded vasopressin
Blinded norepinephrine
Outcomes
Primary Outcome Measures
Incidence between groups of a composite outcome of all-cause mortality, cardiovascular and renal complications after high-risk non-cardiac surgeries
Cardiovascular complications include: stroke, acute myocardial infarction, cardiogenic shock, nonfatal myocardial injury, and ventricular or supraventricular arrhythmias.
Renal complications: Acute renal failure with AKIN stage 1 or higher or renal support therapy.
Secondary Outcome Measures
All-cause mortality
mortality rate of any cause
Acute myocardial infarction
to compare between groups the incidence of acute myocardial infarction
Cardiogenic shock
to compare between groups the incidence of cardiogenic shock
Ventricular and / or supraventricular arrhythmia
to compare between groups the incidence of Ventricular and / or supraventricular arrhythmia
Acute respiratory distress syndrome (ARDS)
to compare between groups the incidence of Acute respiratory distress syndrome (ARDS)
Stroke and transient ischemic attack
to compare between groups the incidence of Stroke and transient ischemic attack
Delirium
to compare between groups the incidence of Delirium
Acute renal failure (AKIN 1 or more)
to compare between groups the incidence of Acute renal failure (AKIN 1 or more)
Length of time in the Intensive Care Unit (ICU) and hospital
Length of time in the Intensive Care Unit (ICU) and hospital
Length of mechanical ventilation
Length of mechanical ventilation
Septic shock
to compare between groups the incidence of septic shock
hospital and ICU readmission rate
hospital and ICU readmission rate
Reoperation
number of patients who required reoperation
Incidence of severe adverse events
to compare the incidence of severe adverse outcomes defined as mesenteric ischemia, digital ischemia, hyponatremia (Na<130mEq/L), myocardial infarction or stroke
Full Information
NCT ID
NCT03483753
First Posted
February 5, 2018
Last Updated
October 2, 2023
Sponsor
University of Sao Paulo
1. Study Identification
Unique Protocol Identification Number
NCT03483753
Brief Title
Vasopressin or Norepinephrine in Vasoplegic Shock After Non-cardiac Surgery
Acronym
VANCSIII
Official Title
Vasopressin or Norepinephrine in Vasoplegic Shock After Non-cardiac Surgery: a Randomized and Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
October 2023
Overall Recruitment Status
Withdrawn
Why Stopped
no funding for the study
Study Start Date
January 2019 (Anticipated)
Primary Completion Date
October 2, 2023 (Actual)
Study Completion Date
October 2, 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo
4. Oversight
Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of the present study is to evaluate the effect of vasopressin compared to norepinephrine on the clinical complications of patients with vasospastic shock after noncardiac surgeries.
Detailed Description
The Systemic Inflammatory Response Syndrome (SIRS) is a common complication after non-cardiac surgery, impacting negatively on patient outcome and with high incidence rates. Vasoplegic syndrome is the most serious complication of SIRS and can happen after any type of surgery. The etiology of the vasoplegic syndrome has not yet been fully elucidated, but is known to occur more frequently in patients at high surgical risk, submitted to major surgeries, or in the presence of perioperative complications and patients with comorbidities. In this circumstance, the depletion of vasopressin stocks is described, which may contribute to the refractoriness of the shock and the lack of response to the catecholaminergic drugs. The standard treatment of perioperative vasoplegia has been adequate volume replacement and administration of vasopressors, with norepinephrine being the most commonly used. However, it is known that norepinephrine may have deleterious effects on the body and in 20% of patients with vasospastic shock it is ineffective. Previous studies have suggested benefits of adding vasopressin in refractory situations, especially in septic shock. Recently the VANCS study (Vasopressin or norepinephrine in the vasopregic shock after cardiac surgery: double-blind, controlled and randomized study) demonstrated superiority of vasopressin in the reversion of vasoplegic shock after cardiac surgery, as well as a lower incidence of renal insufficiency, atrial fibrillation and shorter hospitalization time. (Anesthesiology. 2017 Jan;126(1):85-93.)
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Circulatory Shock, Non-cardiac Surgery
Keywords
Vasopressin, Norepinephrine, Post-operative, Critical Care
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
0 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Vasopressin group
Arm Type
Experimental
Arm Description
Blinded vasopressin
Arm Title
Norepinephrine group
Arm Type
Active Comparator
Arm Description
Blinded norepinephrine
Intervention Type
Drug
Intervention Name(s)
Vasopressin
Other Intervention Name(s)
Blinded Vasopressin
Intervention Description
Blinded Vasopressin will be started if there is persistent hypotension, characterized by mean arterial pressure <65 mmHg after fluid replacement.
Continuous infusion of the drug at doses ranging from 0.01 U / min to 0.06 U / min
Intervention Type
Drug
Intervention Name(s)
Norepinephrine
Other Intervention Name(s)
Blinded Norepinephrine
Intervention Description
Blinded Norepinephrine will be started if there is persistent hypotension, characterized by mean arterial pressure <65 mmHg after fluid replacement. Continuous infusion of the drug at doses ranging from 0.1 mcg / kg / min to 1.0 mcg / kg / min.
Primary Outcome Measure Information:
Title
Incidence between groups of a composite outcome of all-cause mortality, cardiovascular and renal complications after high-risk non-cardiac surgeries
Description
Cardiovascular complications include: stroke, acute myocardial infarction, cardiogenic shock, nonfatal myocardial injury, and ventricular or supraventricular arrhythmias.
Renal complications: Acute renal failure with AKIN stage 1 or higher or renal support therapy.
Time Frame
30 days
Secondary Outcome Measure Information:
Title
All-cause mortality
Description
mortality rate of any cause
Time Frame
30 days after randomization
Title
Acute myocardial infarction
Description
to compare between groups the incidence of acute myocardial infarction
Time Frame
30 days after randomization
Title
Cardiogenic shock
Description
to compare between groups the incidence of cardiogenic shock
Time Frame
30 days after randomization
Title
Ventricular and / or supraventricular arrhythmia
Description
to compare between groups the incidence of Ventricular and / or supraventricular arrhythmia
Time Frame
30 days
Title
Acute respiratory distress syndrome (ARDS)
Description
to compare between groups the incidence of Acute respiratory distress syndrome (ARDS)
Time Frame
30 days
Title
Stroke and transient ischemic attack
Description
to compare between groups the incidence of Stroke and transient ischemic attack
Time Frame
30 days
Title
Delirium
Description
to compare between groups the incidence of Delirium
Time Frame
30 days
Title
Acute renal failure (AKIN 1 or more)
Description
to compare between groups the incidence of Acute renal failure (AKIN 1 or more)
Time Frame
30 days
Title
Length of time in the Intensive Care Unit (ICU) and hospital
Description
Length of time in the Intensive Care Unit (ICU) and hospital
Time Frame
30 days
Title
Length of mechanical ventilation
Description
Length of mechanical ventilation
Time Frame
30 days
Title
Septic shock
Description
to compare between groups the incidence of septic shock
Time Frame
30 days
Title
hospital and ICU readmission rate
Description
hospital and ICU readmission rate
Time Frame
30 days
Title
Reoperation
Description
number of patients who required reoperation
Time Frame
30 days
Title
Incidence of severe adverse events
Description
to compare the incidence of severe adverse outcomes defined as mesenteric ischemia, digital ischemia, hyponatremia (Na<130mEq/L), myocardial infarction or stroke
Time Frame
30 days
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Age greater than 18 years;
Patients undergoing high-risk non-cardiac surgery;
vasopressor need within 24 hours after surgery, defined as mean arterial pressure (MAP) <65 mmHg after volume resuscitation with at least 1 liter of crystalloid solution (Ringer's lactate) and maintaining a cardiac index> 2.2 ml / min / m²;
Signature of the informed consent form.
Exclusion Criteria:
Allergy to vasoactive drugs;
Previous use of vasopressor;
Gestation;
Presence of Raynaud's phenomenon, altered Allen's test, systemic sclerosis or vasospastic diathesis;
Severe hyponatremia (Na <130 mEq / L);
Acute mesenteric ischemia;
Acute coronary syndrome;
Participation in another study;
Refusal to participate in the study.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juliano P Almeida, MD, PhD
Organizational Affiliation
University of Sao Paulo
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Tais F Szeles, MD
Organizational Affiliation
University of Sao Paulo
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
19822810
Citation
Levin MA, Lin HM, Castillo JG, Adams DH, Reich DL, Fischer GW. Early on-cardiopulmonary bypass hypotension and other factors associated with vasoplegic syndrome. Circulation. 2009 Oct 27;120(17):1664-71. doi: 10.1161/CIRCULATIONAHA.108.814533. Epub 2009 Oct 12.
Results Reference
background
PubMed Identifier
11529214
Citation
Landry DW, Oliver JA. The pathogenesis of vasodilatory shock. N Engl J Med. 2001 Aug 23;345(8):588-95. doi: 10.1056/NEJMra002709. No abstract available.
Results Reference
background
PubMed Identifier
27147845
Citation
Gkisioti S, Mentzelopoulos SD. Vasogenic shock physiology. Open Access Emerg Med. 2011 Jan 6;3:1-6. doi: 10.2147/OAEM.S10388. eCollection 2011.
Results Reference
background
PubMed Identifier
19678915
Citation
Teboul JL, Monnet X. Detecting volume responsiveness and unresponsiveness in intensive care unit patients: two different problems, only one solution. Crit Care. 2009;13(4):175. doi: 10.1186/cc7979. Epub 2009 Aug 10.
Results Reference
background
PubMed Identifier
22911566
Citation
Brown SM, Lanspa MJ, Jones JP, Kuttler KG, Li Y, Carlson R, Miller RR 3rd, Hirshberg EL, Grissom CK, Morris AH. Survival after shock requiring high-dose vasopressor therapy. Chest. 2013 Mar;143(3):664-671. doi: 10.1378/chest.12-1106.
Results Reference
background
PubMed Identifier
10411844
Citation
Morales D, Madigan J, Cullinane S, Chen J, Heath M, Oz M, Oliver JA, Landry DW. Reversal by vasopressin of intractable hypotension in the late phase of hemorrhagic shock. Circulation. 1999 Jul 20;100(3):226-9. doi: 10.1161/01.cir.100.3.226.
Results Reference
background
PubMed Identifier
18305265
Citation
Russell JA, Walley KR, Singer J, Gordon AC, Hebert PC, Cooper DJ, Holmes CL, Mehta S, Granton JT, Storms MM, Cook DJ, Presneill JJ, Ayers D; VASST Investigators. Vasopressin versus norepinephrine infusion in patients with septic shock. N Engl J Med. 2008 Feb 28;358(9):877-87. doi: 10.1056/NEJMoa067373.
Results Reference
background
PubMed Identifier
27841820
Citation
Russell JA. Vasopressin, Norepinephrine, and Vasodilatory Shock after Cardiac Surgery: Another "VASST" Difference? Anesthesiology. 2017 Jan;126(1):9-11. doi: 10.1097/ALN.0000000000001435. No abstract available.
Results Reference
background
PubMed Identifier
27841822
Citation
Hajjar LA, Vincent JL, Barbosa Gomes Galas FR, Rhodes A, Landoni G, Osawa EA, Melo RR, Sundin MR, Grande SM, Gaiotto FA, Pomerantzeff PM, Dallan LO, Franco RA, Nakamura RE, Lisboa LA, de Almeida JP, Gerent AM, Souza DH, Gaiane MA, Fukushima JT, Park CL, Zambolim C, Rocha Ferreira GS, Strabelli TM, Fernandes FL, Camara L, Zeferino S, Santos VG, Piccioni MA, Jatene FB, Costa Auler JO Jr, Filho RK. Vasopressin versus Norepinephrine in Patients with Vasoplegic Shock after Cardiac Surgery: The VANCS Randomized Controlled Trial. Anesthesiology. 2017 Jan;126(1):85-93. doi: 10.1097/ALN.0000000000001434.
Results Reference
result
PubMed Identifier
16616623
Citation
Takenaka K, Ogawa E, Wada H, Hirata T. Systemic inflammatory response syndrome and surgical stress in thoracic surgery. J Crit Care. 2006 Mar;21(1):48-53; discussion 53-5. doi: 10.1016/j.jcrc.2005.07.001.
Results Reference
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PubMed Identifier
9403749
Citation
Haga Y, Beppu T, Doi K, Nozawa F, Mugita N, Ikei S, Ogawa M. Systemic inflammatory response syndrome and organ dysfunction following gastrointestinal surgery. Crit Care Med. 1997 Dec;25(12):1994-2000. doi: 10.1097/00003246-199712000-00016.
Results Reference
result
PubMed Identifier
19534818
Citation
Dubin A, Pozo MO, Casabella CA, Palizas F Jr, Murias G, Moseinco MC, Kanoore Edul VS, Palizas F, Estenssoro E, Ince C. Increasing arterial blood pressure with norepinephrine does not improve microcirculatory blood flow: a prospective study. Crit Care. 2009;13(3):R92. doi: 10.1186/cc7922. Epub 2009 Jun 17.
Results Reference
result
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Vasopressin or Norepinephrine in Vasoplegic Shock After Non-cardiac Surgery
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