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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Withdrawn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
University of Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Circulatory Shock focused on measuring Vasopressin, Norepinephrine, Post-operative, Critical Care

Eligibility Criteria

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

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

    First Posted
    February 5, 2018
    Last Updated
    October 2, 2023
    Sponsor
    University of Sao Paulo
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    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
    result
    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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