Hypnosis to Perform Awake Intubation

NCT ID: NCT02513511

Last Updated: 2019-09-27

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

30 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-08-01

Study Completion Date

2019-09-25

Brief Summary

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Awake intubation is a recommended safety procedure in specific cases where the intubation or ventilation before general anesthesia is at risk.

Numerous techniques to allow awake intubation have been described, such as pure awake technique, local anesthetics or intravenous sedation for example.

Hypnosis is used for various operating room techniques and surgeries. The investigators aim to analyze the feasibility of awake laryngoscopy and intubations on patients placed under hypnosis alone.

Detailed Description

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Awake intubation is a recommended safety procedure in specific cases where the intubation or ventilation before general anesthesia is at risk.

Numerous techniques to allow awake intubation have been described, such as pure awake technique, local anesthetics or intravenous sedation for example.

Hypnosis is used for various operating room techniques and surgeries. The investigators aim to analyze the feasibility of awake laryngoscopy and intubations on patients placed under hypnosis alone.

Once patient will consent to be enrolled in the study, the same physician, trained in hypnosis, will accompany the patient in the operating room and place him into a hypnotic state. Once this hypnotic state is achieved, an oro-tracheal laryngoscopy will be performed with an Airtraq videolaryngoscope by an experienced anesthetist, specialised in the management of the difficult airway. If conditions allow it, the laryngoscopy will be followed by an oro-tracheal intubation.

A questionnaire assessing objective and subjective criteria from the patient and from the airway specialist will be collected.

Conditions

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Nasal Obstruction

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Hypnosis

the investigators will put the patient into a hypnotic state and analyze laryngoscopy under hypnosis, followed by intubation.

Group Type EXPERIMENTAL

laryngoscopy under hypnosis

Intervention Type PROCEDURE

patient will be put in an hypnotic state before performing a laryngoscopy followed by oro-tracheal intubation

Interventions

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laryngoscopy under hypnosis

patient will be put in an hypnotic state before performing a laryngoscopy followed by oro-tracheal intubation

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* adults
* american society of anesthesiology classification 1-3
* understanding of french language

Exclusion Criteria

* history of difficult intubation
* patient refusal
* deafness
* uncomfortable with french language understanding
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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University of Lausanne Hospitals

OTHER

Sponsor Role lead

Responsible Party

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Patrick Schoettker,MD PD

MD, PD

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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patrick Schoettker, MD, PD

Role: PRINCIPAL_INVESTIGATOR

University of Lausanne Hospitals

Locations

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Dpt of Anesthesiology, University of Lausanne CHUV

Lausanne, Canton of Vaud, Switzerland

Site Status

Countries

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Switzerland

Other Identifiers

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169/14

Identifier Type: -

Identifier Source: org_study_id

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