Skip to main content
OpenTrials
Recruiting

NCT Number: NCT02986581

Prospective Cohort Study of Rapid Response Team

The purpose of this study is to collect data of rapid response team activated patients prospectively

Recruiting

Interested in participating?

Request Info

Key information

Conditions

Hospital Medical Emergency Team Disease Attributes Emergencies Hospital Rapid Response Team Medicine, Emergency Pathologic Processes Pathological Conditions, Signs and Symptoms

Age range

15 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Seoul National University Bundang Hospital

Seongnam-si, South Korea

Location status: Recruiting

Location contact

Yeon Joo Lee, MD

CONTACT

[email protected]

+82317877082

About this study

acutely deteriorating patients including sudden cardiac arrest in general ward who are monitored and intervened by rapid response team

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients admitted to general ward in Seoul National University Bundang Hospital and monitored by in-hospital rapid response system.

Exclusion criteria

  • patients admitted to pediatric wards
  • patients in emergency room, intensive care unit, and operating room

Treatment and study plan

Primary outcomes

  1. mortality or ICU admission of rapid response team activated patient

    Time frame: an average of 1 year

  2. incidence of preventable cardiac arrest

    Time frame: an average of 1 year

Secondary outcomes

  1. Frequency of triggerring criteria(1) for activation of rapid response team

    Time frame: an average of 1 year

    SBP <90mmHg(mABP 60mmHg) +- clinically correlated symptom or sign

  2. Frequency of triggerring criteria(2) for activation of rapid response team

    Time frame: an average of 1 year

    HR: <50/min or >140/min or symptomatic arrythmia

  3. Frequency of triggerring criteria(3) for activation of rapid response team

    Time frame: an average of 1 year

    RR: <10/min or >30/min or stridor(sign of airway obstruction) or accessary muscle use

  4. Frequency of triggerring criteria(4) for activation of rapid response team

    Time frame: an average of 1 year

    Oxygenation: SaO2 <90% in room air or FM 8L/min

  5. Frequency of triggerring criteria(5) for activation of rapid response team

    Time frame: an average of 1 year

    Metabolic acidosis: Lactic acid<2.5 , TCO2 <15

  6. Frequency of triggerring criteria(6) for activation of rapid response team

    Time frame: an average of 1 year

    ABGA abnormality : PaCO2>50 or pH<7.3 or PaO2<60

  7. Frequency of triggerring criteria(7) for activation of rapid response team

    Time frame: an average of 1 year

    ABGA abnormality : PaCO2>50 or pH<7.3 or PaO2<60

  8. Frequency of triggerring criteria(8) for activation of rapid response team

    Time frame: an average of 1 year

    Any serious concern about overall deterioration detected by doctor, nurse and caregiver at bedside

Study contacts

Contact information is provided by the study sponsor or research team.

Yeon Joo Lee, MD

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Seoul National University Hospital

Other

Collaborators

  • Seoul National University Bundang Hospital

Registry information

Important dates

Study start
2016
Primary completion
2022
Study completion
2026
First posted
Dec 8, 2016
Registry last updated
Jun 30, 2021

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.

Related clinical trials

Published trials that share one or more normalized conditions with this study.