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CompletedNCT01987245PWMQCUpdated Apr 29, 2015

Plethysmographic Waveform for Monitoring the Quality of Cardiopulmonary Resuscitation

An observational study in Cardiopulmonary Arrest, Cardiopulmonary Resuscitation and Return of Spontaneous Circulation, sponsored by Jun Xu. Completed at 1 site in China. Open to participants aged 18 Years to 75 Years. Per ClinicalTrials.gov, last updated 2015-04-29.

Sponsored by Jun Xu · Observational

Study type
Observational
Model
Case-only
Time perspective
Prospective
Enrollment
617
Ages
18 Years to 75 Years
Sex
All
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Study 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.

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Conditions studied

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

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03

In context

Heart Arrest

966 studies on the registry are indexed under Heart Arrest; 227 are open to participants now.

This study's enrollment of 617 is above the median of 200 across 383 observational studies indexed under Heart Arrest.

Browse Heart Arrest studies →

Lead sponsor

Jun Xu is the lead sponsor of 2 studies on the registry; 1 is open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 75 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

emergency room sample of multi-centers

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

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.
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Study design

Observational model
Case-only
Time perspective
Prospective
Enrollment
617 participants (actual)
Patient registry
No
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What researchers measure

Primary outcomes

  1. survival rate

    Time frame: 4 weeks

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Study locations

1 site
  • PUMCH
    Beijing, China
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References and documents

Publications

  • Hu Y, Xu J, Zhu H, Zhang G, Sun F, Zhang Y, Yu X. [Profile and outcome of cardiopulmonary resuscitation after sudden cardiac arrests in the emergency department: a multicenter prospective observational study]. Zhonghua Wei Zhong Bing Ji Jiu Yi Xue. 2018 Mar;30(3):234-239. doi: 10.3760/cma.j.issn.2095-4352.2018.03.009. Chinese. PubMed 29519282 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 29, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01987245
Lead sponsor
Jun Xu
Responsible party
Jun Xu (Emergency Department, Peking Union Medical College Hospital) — Sponsor-investigator
First posted
Nov 19, 2013
Start date
Jan 2014
Primary completion
Mar 2015
Completion
Mar 2015
Last update
Apr 29, 2015

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2015. You cannot join it, but the record below documents what was studied.

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