NCT01987245

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.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
617

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jan 2014

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 5, 2013

Completed
14 days until next milestone

First Posted

Study publicly available on registry

November 19, 2013

Completed
1 month until next milestone

Study Start

First participant enrolled

January 1, 2014

Completed
1.2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 1, 2015

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 1, 2015

Completed
Last Updated

April 29, 2015

Status Verified

April 1, 2015

Enrollment Period

1.2 years

First QC Date

November 5, 2013

Last Update Submit

April 27, 2015

Conditions

Cardiopulmonary ArrestCardiopulmonary ResuscitationReturn of Spontaneous CirculationPulse Oximeter Plethysmographic Waveform

Outcome Measures

Primary Outcomes (1)

  • survival rate

    4 weeks

Eligibility Criteria

Age18 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

emergency room sample of multi-centers

You may qualify if:

  • 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

You may not qualify if:

  • 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)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

PUMCH

Beijing, China

Location

Related Publications (1)

  • 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.

    PMID: 29519282DERIVED

MeSH Terms

Conditions

Heart Arrest

Condition Hierarchy (Ancestors)

Heart DiseasesCardiovascular Diseases

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Emergency Department

Study Record Dates

First Submitted

November 5, 2013

First Posted

November 19, 2013

Study Start

January 1, 2014

Primary Completion

March 1, 2015

Study Completion

March 1, 2015

Last Updated

April 29, 2015

Record last verified: 2015-04

Locations

CN(1)