SEVOflurane Inhalation in CARdiac Arrest Resuscitated Patients Treated With Therapeutic Hypothermia

NCT ID: NCT02201134

Last Updated: 2025-07-14

Study Results

Results pending

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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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-07-31

Study Completion Date

2017-12-31

Brief Summary

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Studying the feasibility of an initial sedation with inhalated sevoflurane during therapeutic hypothermia of cardiac arrests resuscitated patients.

Detailed Description

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Prospective clinical study in ICU with ventilated patients sedated with sevoflurane using the Mirus® and Anaconda® , establishing the feasibility of an initial sedation of patients resuscitated from cardiac arrest and treated with therapeutic hypothermia.

Conditions

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Cardiac Arrest Therapeutic Hypothermia

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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sevoflurane

Group Type OTHER

sevoflurane

Intervention Type DRUG

Interventions

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sevoflurane

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* -Adult patients ventilated requiring therapeutic hypothermia in ICU
* Stable respiratory and hemodynamic conditions
* Epinephrine and norepinephrine infusion rate \< 1,5 g/kg/min
* Consent of patients or family
* Arterial line
* Patients resuscitated after cardiac arrest
* No Flow \< 10 min
* Low Flow \< 20 min
* Neutropenia \< 1 G/L
* Post traumatic cardiac arrest
* Contraindication of halogenated anesthesics
* Extra corporeal life support or intra aortic balloon pump

Exclusion Criteria

* -Pregnant woman
* Hemodynamic instability
* Brain death defined by the disappearance of brain stem reflexes
Minimum Eligible Age

18 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University Hospital, Estaing

OTHER

Sponsor Role collaborator

Hopital Gabriel Montpied

OTHER

Sponsor Role collaborator

University Hospital, Clermont-Ferrand

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Sébastien PERBET

Role: PRINCIPAL_INVESTIGATOR

University Hospital, Clermont-Ferrand

Locations

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CHU de Clermont-Ferrand

Clermont-Ferrand, , France

Site Status

Countries

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France

Other Identifiers

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2014-001196-31

Identifier Type: -

Identifier Source: secondary_id

CHU-0199

Identifier Type: -

Identifier Source: org_study_id

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