NCT02986581

Brief Summary

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

Trial Health

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
79,800

participants targeted

Target at P75+ for all trials

Timeline
6mo left

Started Nov 2016

Longer than P75 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress95%
Nov 2016Nov 2026

Study Start

First participant enrolled

November 1, 2016

Completed
3 days until next milestone

First Submitted

Initial submission to the registry

November 4, 2016

Completed
1 month until next milestone

First Posted

Study publicly available on registry

December 8, 2016

Completed
5.9 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2022

Completed
4 years until next milestone

Study Completion

Last participant's last visit for all outcomes

November 1, 2026

Expected
Last Updated

June 30, 2021

Status Verified

June 1, 2021

Enrollment Period

6 years

First QC Date

November 4, 2016

Last Update Submit

June 27, 2021

Conditions

Hospital Medical Emergency TeamMedicine, EmergencyHospital Rapid Response Team

Outcome Measures

Primary Outcomes (2)

  • mortality or ICU admission of rapid response team activated patient

    an average of 1 year

  • incidence of preventable cardiac arrest

    an average of 1 year

Secondary Outcomes (8)

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

    an average of 1 year

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

    an average of 1 year

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

    an average of 1 year

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

    an average of 1 year

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

    an average of 1 year

  • +3 more secondary outcomes

Eligibility Criteria

Age15 Years+
Sexall
Healthy VolunteersNo
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

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

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Seoul National University Bundang Hospital

Seongnam-si, South Korea

RECRUITING

MeSH Terms

Conditions

Emergencies

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Officials

  • Yeon Joo Lee, MD

    Seoul National University Bundang Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Yeon Joo Lee, MD

CONTACT

yjlee1117@snubh.org

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Target Duration
3 Months
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

November 4, 2016

First Posted

December 8, 2016

Study Start

November 1, 2016

Primary Completion

November 1, 2022

Study Completion (Estimated)

November 1, 2026

Last Updated

June 30, 2021

Record last verified: 2021-06

Locations

KR(1)