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Идёт набор NCT07365137

Prospective Evaluation of Foreign Body Airway Obstruction Interventions Among Adults and Children

Наблюдательное Foreign Body Airway Obstruction

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Abdominal thrust, Back blows, Chest compressions/thrusts.
Кому может быть актуально
Состояния в реестре: Foreign Body Airway Obstruction. Базовые параметры: от 3 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Канада
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Prospective Evaluation of Foreign Body Airway Obstruction Interventions Among Adults and Children: A Non-randomized Pilot Cohort Study

Обзор

Foreign body airway obstruction (FBAO, choking) is a life-threatening emergency requiring time-sensitive treatment to prevent severe injury or deaths. Traditional treatments taught in first aid courses include abdominal thrusts, back blows, and chest compressions or thrusts. Currently, first aid guidelines recommend different treatments for adults, child and infants. Until recently, data on these techniques was limited to case series from the late 1900's. To further improve our knowledge of which treatment is most effective and safest for patients, this study will collect data on choking incidents in Alberta, Canada. The first phase of this project will make sure identifying and recruiting choking patients in real-time is possible so that the highest quality of data can be collected. If successful, this study will support a future project where the different choking treatments are compared in terms of their effectiveness and safety. This study will focus on adults and children over the age of 2 years.

Вмешательства

  • Процедура Abdominal thrust
    Abdominal thrust received as first intervention
  • Процедура Back blows
    Back blows received as first intervention
  • Процедура Chest compressions/thrusts
    Chest compressions or thrusts received as first intervention

Первичные конечные точки

  • Eligible patient recruitment [Срок оценки: Through study completion, a 6 month period]
Вторичные конечные точки (6)
  • Proportion of eligible patients recruited [Срок оценки: Through study completion, a 6 month period]
  • Proportion of recruited patients with satisfactory data collection [Срок оценки: Through study completion, a 6 month period]
  • Foreign body airway obstruction relief [Срок оценки: Day 1]
  • Survival to acute care discharge [Срок оценки: From date of enrolment until the date of acute care discharge or date of death from any cause, whichever came first, assessed up to 3 month]
  • Survival to acute care discharge with favourable neurological outcome [Срок оценки: From date of enrolment until the date of acute care discharge or date of death from any cause, whichever came first, assessed up to 3 month]
  • Intervention-associated injuries [Срок оценки: From date of enrolment until the date of acute care discharge or date of death from any cause, whichever came first, assessed up to 3 month]

Критерии участия

Критерии включения

  • Adult or children (aged greater than 2 years) who experienced an out-of-hospital FBAO in Alberta, Canada
  • Received a FBAO intervention while conscious by bystander or healthcare provider
  • Were assessed by EMS at the time of the incident, or later attended an emergency department due to the incident

Критерии исключения

  • Patients with abnormal airway anatomy such as a tracheostomy.
  • Patients who were unconscious when they received the initial FBAO intervention

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Когортное

Центры проведения

Канада · 1 центр
  • Virtual — Calgary

Идентификаторы

NCT: NCT07365137 · REB25-0419A

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗