Plethysmographic Waveform for Monitoring the Quality of Cardiopulmonary Resuscitation

Completed

• Conditions: Cardiopulmonary Arrest; Pulse Oximeter Plethysmographic Waveform; Return of Spontaneous Circulation; Cardiopulmonary Resuscitation

• Registration Number: NCT01987245
• Lead Sponsor: Jun Xu

Brief Summary

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.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2013-11-05
• Study First Submitted QC: 2013-11-12
• Study First Posted: 2013-11-19
• Study Start: 2014-01
• Primary Completion: 2015-03
• Study Completion: 2015-03
• Status Verified: 2015-04
• Last Update Submitted: 2015-04-27
• Last Update Posted: 2015-04-29

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 617

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 & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
survival rate	4 weeks

Trial Locations

Locations (1)

PUMCH; 🇨🇳 Beijing, China