Cardiac Output Response to Vasopressin Infusion In Abdominal Surgery Patients Under Mechanical Ventilation
NCT ID: NCT04935814
Last Updated: 2022-12-05
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE4
20 participants
INTERVENTIONAL
2021-06-09
2022-08-02
Brief Summary
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Detailed Description
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Monitoring of cardiac output and stroke volume is a valuable and essential aid in determining the therapies to be used for this optimization, whether it involves volume expansion or the use of a vasopressor or even inotropic agent.
Several vasopressor therapies have been available to date. Norepinephrine is currently the reference in the treatment of vasoplegic shock states, but also in the operating room during major surgery or in fragile patients. Other molecules are currently available and are used in a disparate manner, according to the habits of each practitioner, sometimes outside regulatory rules, not following international recommendations concerning the pathology in question: adrenaline, dopamine, phenylephrine, terlipressin...
Vasopressin (D-arginine-D-vasopressin) is an endogenous hormone synthesized by the hypothalamus (peptide composed of 9 amino acids) which has an antidiuretic renal action through its V2 receptor but also a vasoconstriction activity through its V1a receptor, at the level of the smooth muscles of the vascular wall. It also participates in the stimulation of catecholamine secretion by the adrenal medulla. Vasopressin is commercially available under the name "argipressin". It is currently indicated as an adjunct to other vasopressors such as norepinephrine in refractory septic shock to maintain satisfactory hemodynamic stability.
However, its vasoconstrictive and hemodynamic effects, including its influence on cardiac output, have never been studied to date and to the knowledge of investigators. In particular, there are no studies showing the influence of this molecule on mean systemic pressure and venous return resistance, which are fundamental determinants of its impact on left heart function and thus on cardiac output.
In this study, the investigators propose to explore the hemodynamic variations induced by vasopressin and its influence on cardiac output, mean systemic pressure, and venous return resistance measured through cardiopulmonary interactions, according to the approach proposed by Guyton.
Conditions
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Study Design
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NA
SEQUENTIAL
BASIC_SCIENCE
NONE
Sequential positions of patients will be randomized.
Study Groups
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Continuous vasopressin infusion
After general anesthesia, patients will receive a continuous infusion of vasopressin in order to improve mean arterial pressure by 20 mmHg.
Vasopressin, Arginine
Once vasopressin infusion started, patients positions will be randomized: Trendelenburg (-30°), anti Trendelenburg (+30°) and supine position (0°).
Interventions
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Vasopressin, Arginine
Once vasopressin infusion started, patients positions will be randomized: Trendelenburg (-30°), anti Trendelenburg (+30°) and supine position (0°).
Eligibility Criteria
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Inclusion Criteria
* Planned for a major abdominal surgery under general anesthesia
* Under mechanical ventilation
* Presence of a central venous and arterial lines allowing transpulmonary thermodilution cardiac output measurement
* Patient's consent with a social insurance
Exclusion Criteria
* History of heart attack, arteriopathy or aneurysm
* Contraindication to use transpulmonary thermodilution to measure cardiac output :
* coagulopathy
* cardiac arrythmia
* presence of pace-maker or defibrillator
* severe valvulopathy
* Patients with Acute Respiratory Distress Syndrome (according to Berlin criteria)
* History of arterial hypertension (treated or not)
* History of seizure, chronic headache, asthma or heart failure
* Left Ventricular Ejection Fraction (LVEF) \< 45% or right ventricular dysfunction
* History of pulmonary lobectomy or surgery
* History of restrictive or obstructive pulmonary disease
* Body Mass Index (BMI) \< 15 or \> 40 kg/m²
* Pregnancy
* Known allergy to vasopressin
* Patients under protection of justice (guardianship, curators...)
18 Years
ALL
No
Sponsors
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University Hospital, Clermont-Ferrand
OTHER
Responsible Party
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Principal Investigators
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Thomas Godet
Role: PRINCIPAL_INVESTIGATOR
University Hospital, Clermont-Ferrand
Locations
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CHU
Clermont-Ferrand, , France
Countries
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Other Identifiers
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CORVaso / RBHP 2021 GODET 2
Identifier Type: -
Identifier Source: org_study_id
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