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Completed

NCT Number: NCT04141267

Inhaled Sedation Using the Anesthetic-conserving Device ( ANACONDA) in Prehospital Emergency Medecine.

Achieving the optimal sedation level for patient management is not always possible using our standard intravenous medications in Pre-hospital Emergency medicine. Inhaled sedation is possible with the Anesthetic-conserving device with a standard respirator.

The pharmacodynamics and pharmacokinetics of halogenated agents allow deep sedation quickly after absorption.

The feasibility of inhaled sedation has never been studied in hospital.

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Key information

Conditions

Endotracheal Intubation Deep Sedation

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHRU de Brest

Brest, 29609, France

About this study

Retrospecive clinical monocentric study with sedated ventilated patients with isoflurane with the AnaConda® system out of hospital.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient sedated by isoflurane with Anesthetic-conserving device in pre-hospital
  • Major patient
  • not opposed to participating

Exclusion criteria

  • Adults Under legal protection
  • patient refusal to participate in study

Treatment and study plan

Primary outcomes

  1. depth of sedation

    Time frame: up to 1 day

    depth of sedation (measured by the Ramsay Score) 10 minutes from start of the sedation and at stop of pre hospital sedation. The Ramsay score ranges level of sedation from 1(patient anxious ,agitated,restless) to 6 (patient exhibits no response).

Secondary outcomes

  1. hemodynamic tolerance of patients during isoflurane sedation

    Time frame: up to 1 day

    comparison of heart rate (heart beats per minute) before isoflurane start and 10 minutes from start of the sedation and at stop of pre hospital sedation

  2. hemodynamic tolerance of patients during isoflurane sedation

    Time frame: up to 1day

    comparison of medium blood pressure (mmHg) before isoflurane start and 10 minutes from start of the sedation and at stop of pre hospital sedation

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Official study title

Feasibility of Isoflurane Sedation Using an Anesthetic-conserving Device in Prehospital Emergency Medicine: A Retrospective Study

Acronym: ANACONDA

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Oct 28, 2019
Registry last updated
Oct 28, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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