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Completed

NCT Number: NCT03351920

Ventilation's Parameters Applied in Emergency Medicine. A Prospective Observational Study

To prospectively assess the mechanical ventilation management when its provided by Emergency Physicians in French Hospital, and to assess complications and outcome of these patients.

The study could be measure the proportion of patients developing an Acute Respiratory Failure Distress after a take care of by French Emergency Departments.

Completed

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Key information

Conditions

Mechanical Ventilation Acute Respiratory Distress Syndrome Lung Diseases Protective Ventilation Respiration Disorders Respiratory Distress Syndrome Respiratory Tract Diseases Survival

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Pierre-Arnaud Fort, Agen, France

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age equal or over 18 years old
  • Needing a invasive or noninvasive mechanical ventilation
  • Mechanical ventilation initiated in Prehospital or IntraHospital Emergency Department by an Emergency Physician

Exclusion criteria

  • Age under 18 years old

Treatment and study plan

Mechanical ventilation

Other

All patients who need an invasive or non invasive mechanical ventilation, initiated in Prehospital or IntraHospital Emergency Department by an emergency Physician

Primary outcomes

  1. Proportion of patients benefiting of a early low-volume ventilation initiated Emergency Department or Prehospital Care.

    Time frame: Day 1

    Early Low volume ventilation will be defined according to a VtE < 8mL/lg

Secondary outcomes

  1. Proportion of patients benefiting of an early protective ventilation in Emergency Departments

    Time frame: Day 1

  2. Proportion of patients with acute respiratory distress syndrome according to the Berlin Definition during the first eight days of following.

    Time frame: from Day 1 to Day 8 and Day 28

    ARDS will be defined according to the Berlin definition.

  3. Proportion of survival from day 1 to Day 8, and to day 28

    Time frame: from Day 1 to Day 8 and Day 28

  4. Indication to mechanical ventilation in Prehospital care and Emergency Departments

    Time frame: Day 1

  5. Mechanical Ventilation Duration in Emergency Departments

    Time frame: Day 1

  6. Mechanical ventilation settings in Emergency Departments

    Time frame: Day 1

    Recorded settings will be Ventilation mode, Tidal volume or Pressure Support Positive End Expiratory Pressure, Ventilation Rate, I : E ratio or Inspiratory Flow or Inspiratory Time.

Sponsors and collaborators

Lead sponsor

Poitiers University Hospital

Other

Registry information

Official study title

Ventilation's Parameters Applied in Emergency Medicine. Observational Study

Acronym: PARAVENT

Important dates

Study start
2017
Primary completion
2019
Study completion
2019
First posted
Nov 24, 2017
Registry last updated
Feb 7, 2020

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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