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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01987245
Other study ID # 2013S-512
Secondary ID 2011-4001-04
Status Completed
Phase N/A
First received November 5, 2013
Last updated April 27, 2015
Start date January 2014
Est. completion date March 2015

Study information

Verified date April 2015
Source Peking Union Medical College Hospital
Contact n/a
Is FDA regulated No
Health authority China: Ministry of Health
Study type Observational

Clinical Trial 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.


Recruitment information / eligibility

Status Completed
Enrollment 617
Est. completion date March 2015
Est. primary completion date March 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility 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

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
China PUMCH Beijing

Sponsors (1)

Lead Sponsor Collaborator
Jun Xu

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary survival rate 4 weeks Yes
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