Hypnosis to Perform Awake Intubation (Hypnotube)
Hypnosis as a Sole Agent to Perform Awake Intubation
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.
調査の概要
詳細な説明
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.
研究の種類
入学 (実際)
段階
- 適用できない
連絡先と場所
研究場所
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-
VD
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Lausanne、VD、スイス、1011
- Dpt of Anesthesiology, University of Lausanne CHUV
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参加基準
適格基準
就学可能な年齢
健康ボランティアの受け入れ
受講資格のある性別
説明
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
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:支持療法
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
|
実験的:Hypnosis
the investigators will put the patient into a hypnotic state and analyze laryngoscopy under hypnosis, followed by intubation.
|
patient will be put in an hypnotic state before performing a laryngoscopy followed by oro-tracheal intubation
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of participants in which laryngoscopy is possible under hypnosis
時間枠:60 minutes
|
laryngoscopy is feasible under hypnosis alone
|
60 minutes
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Number of participants in which intubation is possible under hypnosis
時間枠:60 minutes
|
intubation is feasible under hypnosis alone
|
60 minutes
|
|
comfort assessed by patient
時間枠:60 minutes
|
assessment of comfort on scale 1-5
|
60 minutes
|
|
comfort assessed by doctor
時間枠:60 minutes
|
assessment of comfort on scale 1-5
|
60 minutes
|
協力者と研究者
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (実際)
研究の完了 (実際)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (見積もり)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。