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Determination of the Optimal Dose of Ephedrine in Intraoperative Arterial Hypotension of Newborns and Infants up to 6 Months of Age. (EPHEDRINE)

Primary Purpose

Intraoperative Arterial Hypotension, Infant, Newborn

Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
Ephedrine 30mg/10mL injectable solution, single administration, dose : 0.6, 0.8, 1.0, 1.2 and 1.4 mg/kG
Ephedrine 30mg/10mL injectable solution, single administration, dose : 0.1 mg/kG.
Sponsored by
Hospices Civils de Lyon
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Intraoperative Arterial Hypotension focused on measuring pediatric, intraoperative arterial hypotension, ephedrine, general anesthesia

Eligibility Criteria

undefined - 6 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Newborns or infants < 6 months of age,
  • boys and girls,
  • premature or not,
  • requiring general anesthesia induced by sevoflurane
  • who presents during anesthesia a decrease of blood pressure superior to 20% of the basal mBP (measured prior to surgery) despite of vascular filling with sodium chloride 0.9% (10mL/kg during 10 min).
  • Written, informed consent obtained from the 2 parents

Exclusion Criteria:

  • Allergy to Ephedrine.
  • Emergency surgery.
  • Patient having previously received other vasopressive amines.
  • Use of other indirect sympathomimetic drug such as phenylpropanolamine, phenylephrine, pseudoephedrine and methylphenidate.
  • Premedication with clonidine
  • Congenital heart disease
  • IV-induced anesthesia.

Sites / Locations

  • Hôpital d'Estaing
  • Hospices Civils de Lyon
  • Hôpital Nord

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Ephedrine, dose : 0.6, 0.8, 1.0, 1.2 and 1.4 mg/kG

Ephedrine, dose : 0.1 mg/kG, reference dose

Arm Description

Dose escalation: 6 successive cohorts with a maximal increasing dose

Reference dose

Outcomes

Primary Outcome Measures

Therapeutic success is defined as a mBP superior to 55% of the basal mBP (prior to anesthesia) within 10 minutes post Ephedrine administration

Secondary Outcome Measures

Return to a mBP superior to 38mmHg within 10 minutes post Ephedrine administration
Variations of O2 saturation in cerebral tissue (number of desaturations, evolution under treatment) using a Near Infrared Spectroscopy (NIRS) technology
Tolerance of Ephedrine: occurrence of serious adverse events
Clinical examination focusing specifically on heart rate and hypertension

Full Information

First Posted
February 27, 2015
Last Updated
July 26, 2021
Sponsor
Hospices Civils de Lyon
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1. Study Identification

Unique Protocol Identification Number
NCT02384876
Brief Title
Determination of the Optimal Dose of Ephedrine in Intraoperative Arterial Hypotension of Newborns and Infants up to 6 Months of Age.
Acronym
EPHEDRINE
Official Title
Determination of the Optimal Dose of Ephedrine in Intraoperative Arterial Hypotension of Newborns and Infants up to 6 Months of Age. A Randomized, Controlled, Open-label, Dose Escalation Study.
Study Type
Interventional

2. Study Status

Record Verification Date
July 2021
Overall Recruitment Status
Completed
Study Start Date
June 2015 (Actual)
Primary Completion Date
September 5, 2020 (Actual)
Study Completion Date
September 5, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Hospices Civils de Lyon

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The incidence of arterial hypotension under general anesthesia using sevoflurane is particularly high in newborns and infants up to 6 months of age. A decrease of 20% of the initial mean blood pressure (mBP) is the definition of significant arterial hypotension in adults and children. In adults, intraoperative arterial hypotension is associated with an increase of intraoperative mortality and a certain neurological morbidity. In infants under 6 months of age, neurological disorders have been reported following general anesthesia. Neurotoxicity of hypnotics is often incriminated as should be the episodes of arterial hypotension. Current management of hypotension uses vascular filling with crystalloids and vasopressive amines in second intention. Dopamine is the most frequently used amine. Ephedrine can also be used. Ephedrine is particularly interesting because of its action on both α and β receptors and its mode of administration: one dose and peripheral access. Only one study is available in children from birth to adulthood; it demonstrates a lower hemodynamic response in infants than in adults, when administered a low dose of Ephedrine (0.1 to 0.2 mg/kg). A recent retrospective cohort suggests an under efficacy of low doses and the use of higher doses than those recommended. The primary objective is to determine the optimal dose of ephedrine (dose of ephedrine associated with a difference of proportion of newborns/infants in therapeutic success of 55%) compare to the reference dose of 0.1mg/kg as a first line treatment of intraoperative arterial hypotension. Secondary objectives: Return to a mBP superior to 38mmHg post Ephedrine administration. To assess occurrence of hypoxemic events during anesthesia. To assess tolerance of ephedrine. One hundred and twenty newborn and infants up to 6 months of age will be recruited in 3 sites of the Rhone Alpes Auvergne area over 24 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Intraoperative Arterial Hypotension, Infant, Newborn
Keywords
pediatric, intraoperative arterial hypotension, ephedrine, general anesthesia

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
120 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Ephedrine, dose : 0.6, 0.8, 1.0, 1.2 and 1.4 mg/kG
Arm Type
Experimental
Arm Description
Dose escalation: 6 successive cohorts with a maximal increasing dose
Arm Title
Ephedrine, dose : 0.1 mg/kG, reference dose
Arm Type
Active Comparator
Arm Description
Reference dose
Intervention Type
Drug
Intervention Name(s)
Ephedrine 30mg/10mL injectable solution, single administration, dose : 0.6, 0.8, 1.0, 1.2 and 1.4 mg/kG
Intervention Type
Drug
Intervention Name(s)
Ephedrine 30mg/10mL injectable solution, single administration, dose : 0.1 mg/kG.
Primary Outcome Measure Information:
Title
Therapeutic success is defined as a mBP superior to 55% of the basal mBP (prior to anesthesia) within 10 minutes post Ephedrine administration
Time Frame
Continuous monitoring within 10 minutes post-administration
Secondary Outcome Measure Information:
Title
Return to a mBP superior to 38mmHg within 10 minutes post Ephedrine administration
Time Frame
Continuous monitoring within 10 minutes post-administration
Title
Variations of O2 saturation in cerebral tissue (number of desaturations, evolution under treatment) using a Near Infrared Spectroscopy (NIRS) technology
Time Frame
Continuous monitoring within 10 minutes post-administration
Title
Tolerance of Ephedrine: occurrence of serious adverse events
Description
Clinical examination focusing specifically on heart rate and hypertension
Time Frame
During 3 days post-administration

10. Eligibility

Sex
All
Maximum Age & Unit of Time
6 Months
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Newborns or infants < 6 months of age, boys and girls, premature or not, requiring general anesthesia induced by sevoflurane who presents during anesthesia a decrease of blood pressure superior to 20% of the basal mBP (measured prior to surgery) despite of vascular filling with sodium chloride 0.9% (10mL/kg during 10 min). Written, informed consent obtained from the 2 parents Exclusion Criteria: Allergy to Ephedrine. Emergency surgery. Patient having previously received other vasopressive amines. Use of other indirect sympathomimetic drug such as phenylpropanolamine, phenylephrine, pseudoephedrine and methylphenidate. Premedication with clonidine Congenital heart disease IV-induced anesthesia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mathilde de Queiroz Siqueira, MD
Organizational Affiliation
Service d'anesthésie pédiatrique et obstétricale, Hôpital Femme Mère Enfant, 59 boulevard Pinel - 69 677 BRON Cedex
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hôpital d'Estaing
City
Clermont-Ferrand
ZIP/Postal Code
63003
Country
France
Facility Name
Hospices Civils de Lyon
City
Lyon
Country
France
Facility Name
Hôpital Nord
City
Saint Etienne
ZIP/Postal Code
42055
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
33712076
Citation
Szostek AS, Boucher P, Subtil F, Zerzaihi O, Saunier C, de Queiroz Siqueira M, Merquiol F, Martin P, Granier M, Gerst A, Lambert A, Storme T, Chassard D, Nony P, Kassai B, Gaillard S. Determination of the optimal dose of ephedrine in the treatment of arterial hypotension due to general anesthesia in neonates and infants below 6 months old: the ephedrine study protocol for a randomized, open-label, controlled, dose escalation trial. Trials. 2021 Mar 12;22(1):208. doi: 10.1186/s13063-021-05155-2.
Results Reference
derived

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Determination of the Optimal Dose of Ephedrine in Intraoperative Arterial Hypotension of Newborns and Infants up to 6 Months of Age.

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