Plethysmographic Waveform for Monitoring the Quality of Cardiopulmonary Resuscitation (PWMQC)

This study is not yet open for participant recruitment. (see Contacts and Locations)
Verified September 2014 by Peking Union Medical College Hospital
Sponsor:
Information provided by (Responsible Party):
Jun Xu, Peking Union Medical College Hospital
ClinicalTrials.gov Identifier:
NCT01987245
First received: November 5, 2013
Last updated: September 9, 2014
Last verified: September 2014
  Purpose

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.


Condition
Cardiopulmonary Arrest
Cardiopulmonary Resuscitation
Return of Spontaneous Circulation
Pulse Oximeter Plethysmographic Waveform

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: The Application Research of Plethysmographic Waveform in Quality Control Feedback System During Cardiopulmonary Resuscitation

Resource links provided by NLM:


Further study details as provided by Peking Union Medical College Hospital:

Primary Outcome Measures:
  • survival rate [ Time Frame: 4 weeks ] [ Designated as safety issue: Yes ]

Estimated Enrollment: 600
Study Start Date: January 2014
Estimated Study Completion Date: December 2014
Estimated Primary Completion Date: December 2014 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years to 75 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

emergency room sample of multi-centers

Criteria

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.
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

No Contacts or Locations Provided
  More Information

No publications provided

Responsible Party: Jun Xu, Emergency Department, Peking Union Medical College Hospital
ClinicalTrials.gov Identifier: NCT01987245     History of Changes
Other Study ID Numbers: 2013S-512, 2011-4001-04
Study First Received: November 5, 2013
Last Updated: September 9, 2014
Health Authority: China: Ministry of Health

Additional relevant MeSH terms:
Heart Arrest
Heart Diseases
Cardiovascular Diseases

ClinicalTrials.gov processed this record on September 18, 2014