- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01214460
Impact of Medical Emergency Team and EMS in Tampere University Hospital
September 26, 2019 updated by: Tampere University Hospital
Impact of Medical Emergency Team and EMS on ICU Readmissions and Sudden Cardiac Arrests in Tampere University Hospital
Patients in general wards have abnormal physical values preceding in-hospital cardiac arrest or a transfer to intensive care unit (ICU).
The purpose of Medical Emergency Team (MET) or EMS is to interfere early enough in deteriorating patient status to prevent adverse outcomes like cardiac arrest or transfer to intensive care unit.
The aims of this study are to record and analyze the effects of EMS and department of emergency and both afferent and efferent limbs of MET activity in Finnish tertiary Hospital.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
10000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Pirkanmaa
-
Tampere, Pirkanmaa, Finland, 33521
- Tampere University Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
All adult EMS or in-hospital patients with deteriorating vital signs or patients in risk in Tampere University Hospital
Description
Inclusion Criteria:
- 18 yrs or older
Exclusion Criteria:
- under 18 yrs
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
---|
All MET calls
We make an Utstein type analyze to all MET calls
|
All EMS calls
We make an Utstein type analyze to all EMS calls during June 2015
|
All patient in the emergency department
We make an Utstein type analyze to all Emergency visits during June 2015
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
In-hospital mortality
Time Frame: patients are followed until death
|
patients are followed until death
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The rates of ICU readmissions
Time Frame: one month to six year
|
one month to six year
|
|
The rates of DNAR orders
Time Frame: one month to six year
|
one month to six year
|
|
The number of patients EMS or medical emergency team is called to treat
Time Frame: one month to six years
|
We are going to analyze the number of MET calls and their impact on sudden cardiac arrests in TAUH.
The time frame is 1st Jan 2010 -31st Dec 2015.
It is known fact that well working MET team inside the hospital should decrease the sudden cardiac arrests.
We also analyze the EMS calls and the ED visits in June 2015 to see if patient detoriation is related to sudden in-hospital death.
|
one month to six years
|
Patient mortality after 6 mo of discharge
Time Frame: one month to six year
|
The patients are followed 6 mo after hospital discharge which has happened in year 2010
|
one month to six year
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Sanna Hoppu, MD, PhD, Tampere University Hospital
- Principal Investigator: Jari Kalliomäki, MD, Tampere University Hospital
- Principal Investigator: Joonas Tirkkonen, MD, Tampere University Hospital
- Principal Investigator: Timo Kontula, MD, Tampere University Hospital
- Principal Investigator: Eetu Loisa, Tampere University Hospital
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 2010
Primary Completion (Actual)
July 1, 2016
Study Completion (Actual)
September 26, 2019
Study Registration Dates
First Submitted
July 5, 2010
First Submitted That Met QC Criteria
October 1, 2010
First Posted (Estimate)
October 5, 2010
Study Record Updates
Last Update Posted (Actual)
September 27, 2019
Last Update Submitted That Met QC Criteria
September 26, 2019
Last Verified
September 1, 2019
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- R10111
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Death, Sudden,Cardiac
-
Unity Health TorontoSunnybrook Health Sciences Centre; University of British Columbia; Alberta Health... and other collaboratorsCompleted
-
University Hospital Southampton NHS Foundation...WithdrawnCardiac Arrest | Sudden Death, Cardiac
-
Solae, LLCProvident Clinical ResearchCompletedCardiovascular Disease | Sudden Cardiac Death | Sudden Cardiac Arrest
-
Zoll Medical CorporationTerminatedSudden Cardiac Death | Sudden Cardiac ArrestUnited States
-
Solae, LLCProvident Clinical ResearchCompletedCardiovascular Disease | Sudden Cardiac Death | Sudden Cardiac ArrestUnited States
-
Assistance Publique - Hôpitaux de ParisMinistry of Health, FranceRecruitingHeart Failure | Implantable Cardioverter Defibrillator | Primary Prevention of Sudden Cardiac DeathFrance
-
Zoll Medical CorporationCompletedHeart Failure | Sudden Cardiac Death | Sudden Cardiac Arrest | Heart Failure Low OutputFrance, United States, Germany, Austria
-
University of LuebeckProf. Jürgen Kuschyk, M.D; Giovanni Forleo, M.D.; Mauro Biffi, M.D.RecruitingSudden Cardiac DeathGermany
-
Deutsches Herzzentrum MuenchenCompletedSudden Cardiac DeathGermany
-
Jingfeng WangFudan University; The Affiliated Nanjing Drum Tower Hospital of Nanjing University... and other collaboratorsEnrolling by invitation