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ONDANSETRON AND EFFECTIVE DOSE IN 50% OF SUBJECTS OF PROPHYLACTIC NOREPINEPHRINE INFUSIONS FOR PREVENTING SPINAL ANESTHESIA-INDUCED HYPOTENSION DURING CESAREAN DELIVERY

Primary Purpose

Hypotension, Anesthesia; Adverse Effect, Spinal and Epidural, Cesarean Section

Status
Unknown status
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Ondansetron 4 MG
0.9% Saline
Sponsored by
Laval University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hypotension focused on measuring Spinal Anesthesia, Hypotension, Vascular, Ondansetron Hydrochloride, Norepinephrine, Vasoconstrictor Agents, Cesarean section, Physiological Effects of Drugs, Molecular Mechanisms of Pharmacological Action

Eligibility Criteria

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

Inclusion Criteria:

  • parturients with a singleton pregnancy at term (37 week's gestation and more)
  • elective cesarean delivery under spinal anesthesia
  • American Society of Anesthesiologists physical status < III

Exclusion Criteria:

  • patient refusal
  • allergy or hypersensitivity to Norepinephrine or Ondansetron
  • Use of monoamine oxidase inhibitors, triptyline or imipramine antidepressants
  • Long QT syndrome or another cause of prolonged QT
  • significant preexisting maternal disease (cardiovascular or cerebrovascular disease or coagulopathy, diabetes mellitus)
  • pre-existing or pregnancy-induced hypertension
  • pathological pregnancy (ruptured membranes, pre-eclampsia, placenta praevia, gestational diabetes)
  • body mass index < 18 or > 40
  • height < 150 or > 180
  • fetal abnormalities
  • contraindication to spinal anesthesia

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    INTERVENTION GROUP - ONDANSETRON

    CONTROL GROUP - NORMAL SALINE

    Arm Description

    2 mL of a solution of Ondansetron containing 2mg/ml in a 3 ml syringe will be given intravenously to a patient five minutes before positioning for induction of spinal anesthesia

    2 mL of 0.9% Saline in a 3 ml syringe will be given intravenously to a patient five minutes before positioning for induction of spinal anesthesia

    Outcomes

    Primary Outcome Measures

    ED50 Norepinephrine
    The effective dose in 50% of subjects (ED50) of a prophylactic norepinephrine infusion for preventing hypotension in patients who received a single dose of intravenous ondansetron 4mg or saline control five minutes before spinal anesthesia for elective cesarean delivery

    Secondary Outcome Measures

    Total consumption of Norepinephrine
    The total consumption of Norepinephrine (mcg/kg) in the two groups (pump infusion and bolus)

    Full Information

    First Posted
    January 7, 2021
    Last Updated
    January 9, 2021
    Sponsor
    Laval University
    Collaborators
    CHU de Quebec-Universite Laval
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    1. Study Identification

    Unique Protocol Identification Number
    NCT04703088
    Brief Title
    ONDANSETRON AND EFFECTIVE DOSE IN 50% OF SUBJECTS OF PROPHYLACTIC NOREPINEPHRINE INFUSIONS FOR PREVENTING SPINAL ANESTHESIA-INDUCED HYPOTENSION DURING CESAREAN DELIVERY
    Official Title
    A PROSPECTIVE, RANDOMIZED, DOUBLE-BLINDED STUDY OF THE EFFECT OF A STANDARD DOSE OF INTRAVENOUS ONDANSETRON ON THE EFFECTIVE DOSE IN 50% OF SUBJECTS OF PROPHYLACTIC NOREPINEPHRINE INFUSIONS FOR PREVENTING SPINAL ANESTHESIA-INDUCED HYPOTENSION DURING CESAREAN DELIVERY
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2021
    Overall Recruitment Status
    Unknown status
    Study Start Date
    June 2021 (Anticipated)
    Primary Completion Date
    August 2021 (Anticipated)
    Study Completion Date
    August 2021 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Laval University
    Collaborators
    CHU de Quebec-Universite Laval

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Product Manufactured in and Exported from the U.S.
    No
    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Spinal anesthesia is the preferred technique for elective cesarean section as per ASA guidelines. Hypotension is the main complication of this technique and is secondary to both sympatholysis and its associated decrease in systemic vascular resistance and to the Bezold-Jarisch reflex, which causes hypotension and bradycardia in response to noxious stimuli detected in the cardiac ventricles. In pregnant patients, spinal anesthesia induced hypotension is worsened by compression of the aorta and inferior vena cava by the gravid uterus. In this setting, hypotension could lead to uteroplacental hypoperfusion and fetal distress. In its 2020 guidelines for enhanced recovery after cesarean section, SOAP states that preventing spinal-induced hypotension is an important strategy to enhance maternal and neonatal outcomes in cesarean delivery Recent studies showed that 5-hydroxytryptamine-3 receptor antagonists, mostly used as nausea and vomiting prophylaxis agents, also contributed to inhibit the Bezold-Jarisch reflex and its associated hemodynamic consequences. Ondansetron is the most studied molecule in this field. Many recent studies and meta-analyses show renewed interest in the use of norepinephrine as a first line agent for preventing and treating spinal anesthesia-induced hypotension in obstetric anesthesia practice instead of phenylephrine. Norepinephrine has the advantage of a better cardiac output and cardiac frequency as compared to phenylephrine without any fetal side effect. The combination of ondansetron and phenylephrine for the prevention of spinal anesthesia-induced hypotension has been studied, but not the combination of ondansetron and norepinephrine. The main objective of this study is to evaluate the sparing effect of a standard dose of ondansetron on norepinephrine consumption during elective cesarean section under spinal anesthesia by determining the effective dose in 50% of subjects (ED50) of a prophylactic norepinephrine infusion after receiving a single dose of 4 mg of ondansetron or a saline control.
    Detailed Description
    Vital signs are measured in the preparation area before entrance in the operation theater. The following measures are taken in the supine position every three minutes for three measures: blood pressure and cardiac frequency. The mean blood pressure and cardiac frequency become the reference measure for each patient. Upon entrance in the operation theater, anesthesia care is given in a standardized manner: Supine positioning of the parturient on the operating table Standard monitoring of vitals signs every minute for the time of the study, including systolic, diastolic an mean blood pressures, cardiac frequency and SpO2 18G intravenous catheter insertion on the forearm Randomization of the patient in one of the two groups followed by blind administration of ondansetron or saline 5 minute wait period before sitting the patient for spinal anesthesia Standardized spinal anesthesia: Whitacre 25G spinal needle, L4-L5 intervertebral space, hyperbaric bupivacaine 12mg + fentanyl 10 mcg + morphine 100 mcg Upon injection of the spinal medication: 1000 ml Ringer lactate coloading and start of the iv norepinephrine infusion upon study protocol. Evaluation of the sensitive block level at 5 and 10 minutes, a level of T6 is needed to start surgery Nausea and vomiting prophylaxis in both groups with metoclopramide 10 mg and dexamethasone 4 mg if no contraindication. Nausea and vomiting per cesarean section will be treated with dimenhydrinate 25 mg Bradycardia (HR below 60) will be treated with atropine 0,4 mg Multimodal post-operative analgesia with intra rectal acetaminophen 1000 mg and indomethacin 100 mg Norepinephrine infusion protocol: The rate of the infusion pump is blindly set in mcg/kg/min by one of the investigators before the entrance of the patient and the anesthesia team in the operating room. The setting is hidden from the main physician at all times and the perfusion is started when the spinal medication is injected. For the first patient of each group (saline and ondansetron) the norepinephrine infusion is started at 0,05 mcg/kg/min until the end of the study Hypotension (as defined as a value inferior or equal to 80% of the systolic blood pressure reference value) is treated by the anesthesiologist with a 4 mcg bolus of norepinephrine from a prepared syringe of norepinephrine 4 mcg/ml Hypertension (as defined as a value superior or equal to 120% of the systolic blood pressure reference value) is treated by stopping the norephineprine infusion and restarting it when the value is inferior to 120% of the reference value. For the following patients, the norepinephrine infusion rate will be adjusted by up and down allocation following the results of the previous patient: if no hypotension occurred (no bolus needed): the infusion rate is decreased by 0,005 mcg/kg/min (for example from 0,05 mcg/kg/min to 0,045 mcg/kg/min) / if at least one hypotension occurred (at least one bolus needed): the infusion rate is increased by 0,005 mcg/kg/min (for example from 0,05 mcg/kg/min to 0,055 mcg/kg/min) The study is stopped at the fetal delivery.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Hypotension, Anesthesia; Adverse Effect, Spinal and Epidural, Cesarean Section
    Keywords
    Spinal Anesthesia, Hypotension, Vascular, Ondansetron Hydrochloride, Norepinephrine, Vasoconstrictor Agents, Cesarean section, Physiological Effects of Drugs, Molecular Mechanisms of Pharmacological Action

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Parallel Assignment
    Model Description
    Randomized blinded parallel assignment
    Masking
    ParticipantCare Provider
    Masking Description
    Studied medication will be administered to the patient after randomization by the investigators (two anesthesia residents or two staff anesthesiologists) who will not be involved in subsequent anesthetic management of the patients. The investigators will also program the infusion rate of norepinephrine at the start of each case and will be the only persons aware of the assigned infusion rate. The investigators will hide the infusion rate with an opaque paper cover over the infusion display during the case. The investigators will also collect all the data during each procedures. To summarize, the anesthesiologist in charge of the patient will not know which treatment will be injected and the rate of the pump infusion
    Allocation
    Randomized
    Enrollment
    60 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    INTERVENTION GROUP - ONDANSETRON
    Arm Type
    Experimental
    Arm Description
    2 mL of a solution of Ondansetron containing 2mg/ml in a 3 ml syringe will be given intravenously to a patient five minutes before positioning for induction of spinal anesthesia
    Arm Title
    CONTROL GROUP - NORMAL SALINE
    Arm Type
    Placebo Comparator
    Arm Description
    2 mL of 0.9% Saline in a 3 ml syringe will be given intravenously to a patient five minutes before positioning for induction of spinal anesthesia
    Intervention Type
    Drug
    Intervention Name(s)
    Ondansetron 4 MG
    Intervention Description
    2 mL of a solution of Ondansetron containing 2mg/ml in a 3 ml syringe will be given intravenously to a patient five minutes before positioning for induction of spinal anesthesia
    Intervention Type
    Drug
    Intervention Name(s)
    0.9% Saline
    Intervention Description
    2 mL of 0,9% Saline in a 3 ml syringe will be given intravenously to a patient five minutes before positioning for induction of spinal anesthesia
    Primary Outcome Measure Information:
    Title
    ED50 Norepinephrine
    Description
    The effective dose in 50% of subjects (ED50) of a prophylactic norepinephrine infusion for preventing hypotension in patients who received a single dose of intravenous ondansetron 4mg or saline control five minutes before spinal anesthesia for elective cesarean delivery
    Time Frame
    At the fetal delivery
    Secondary Outcome Measure Information:
    Title
    Total consumption of Norepinephrine
    Description
    The total consumption of Norepinephrine (mcg/kg) in the two groups (pump infusion and bolus)
    Time Frame
    At the fetal delivery

    10. Eligibility

    Sex
    Female
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: parturients with a singleton pregnancy at term (37 week's gestation and more) elective cesarean delivery under spinal anesthesia American Society of Anesthesiologists physical status < III Exclusion Criteria: patient refusal allergy or hypersensitivity to Norepinephrine or Ondansetron Use of monoamine oxidase inhibitors, triptyline or imipramine antidepressants Long QT syndrome or another cause of prolonged QT significant preexisting maternal disease (cardiovascular or cerebrovascular disease or coagulopathy, diabetes mellitus) pre-existing or pregnancy-induced hypertension pathological pregnancy (ruptured membranes, pre-eclampsia, placenta praevia, gestational diabetes) body mass index < 18 or > 40 height < 150 or > 180 fetal abnormalities contraindication to spinal anesthesia
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Romain LANCHON
    Phone
    +1 418-525-4444
    Ext
    47565
    Email
    romain.lanchon@gmail.com

    12. IPD Sharing Statement

    Plan to Share IPD
    No
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    ONDANSETRON AND EFFECTIVE DOSE IN 50% OF SUBJECTS OF PROPHYLACTIC NOREPINEPHRINE INFUSIONS FOR PREVENTING SPINAL ANESTHESIA-INDUCED HYPOTENSION DURING CESAREAN DELIVERY

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