- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01987245
Plethysmographic Waveform for Monitoring the Quality of Cardiopulmonary Resuscitation (PWMQC)
April 27, 2015 updated by: Jun Xu
The Application Research of Plethysmographic Waveform in Quality Control Feedback System During Cardiopulmonary Resuscitation
Cardiopulmonary resuscitation(CPR) is the key to success for high-quality early cardiopulmonary resuscitation, and its success in the restoration of spontaneous circulation (ROSC), therefore, monitoring the quality of cardiopulmonary resuscitation and early identification ROSC is very important.
Now there is no an easy, non-invasive and real-time method to monitor the quality of CPR.
In this study the investigators hypothesis the pulse oximeter waveform can real-time monitor the quality of CPR ,and feedback the quality of CPR to the physicians.
Study Overview
Status
Completed
Study Type
Observational
Enrollment (Actual)
617
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
-
-
-
Beijing, China
- PUMCH
-
-
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 to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
emergency room sample of multi-centers
Description
Inclusion Criteria:
- cardiopulmonary arrest, without do-not-resuscitation(DNR) patients
- After cardiac arrest, there is no more than 10 minutes until basic life support.
- must be carried out advanced life support (tracheal intubation and end-tidal carbon dioxide monitoring)
- comply with ethical requirements and signed informed consent
Exclusion Criteria:
- DNR patients
- rib fractures
- hemorrhagic shock caused cardiac arrest
- severe anemia, hemoglobin less than 7g/dl
- tension pneumothorax without closed drainage
- pulmonary embolism or pericardial tamponade caused cardiac arrest
- onychomycosis
- people who paint fingernails
- clearly influential peripheral oximetry underlying diseases (such as Raynaud's phenomenon, vasculitis)
- The study physicians believe there is any case is not suitable for inclusion.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
survival rate
Time Frame: 4 weeks
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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, 2014
Primary Completion (Actual)
March 1, 2015
Study Completion (Actual)
March 1, 2015
Study Registration Dates
First Submitted
November 5, 2013
First Submitted That Met QC Criteria
November 12, 2013
First Posted (Estimate)
November 19, 2013
Study Record Updates
Last Update Posted (Estimate)
April 29, 2015
Last Update Submitted That Met QC Criteria
April 27, 2015
Last Verified
April 1, 2015
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2013S-512
- 2011-4001-04 (Other Grant/Funding Number: CHRDS)
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 Cardiopulmonary Resuscitation
-
Chang Gung Memorial HospitalCompleted
-
Unity Health TorontoHeart and Stroke Foundation of Canada; Zoll Medical CorporationCompletedCardiopulmonary ResuscitationCanada
-
University Hospital DubravaCompleted
-
Hallym University Kangnam Sacred Heart HospitalCompletedCardiopulmonary ResuscitationKorea, Republic of
-
Universidade do PortoCentro de Investigação em Tecnologias e Serviços de Saúde (CINTESIS); Rede... and other collaboratorsRecruitingCardiopulmonary ResuscitationPortugal
-
Tampere University HospitalNational Istitute For Health and Welfare, FinlandRecruiting
-
National Taiwan University HospitalCompletedCardiopulmonary ResuscitationTaiwan
-
Medical University of ViennaSt. John's Ambulance, Vienna Austria; Universitäres Simulationszentrum Wien...Completed
-
The Royal Wolverhampton Hospitals NHS TrustCompletedCardiopulmonary ResuscitationUnited Kingdom
-
Peking Union Medical College HospitalUnknownCardiopulmonary ResuscitationChina