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
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
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
NCT ID
NCT04703088
First Posted
January 7, 2021
Last Updated
January 9, 2021
Sponsor
Laval University
Collaborators
CHU de Quebec-Universite Laval
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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