- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03769740
Cerebral Oximetry and NIRS in Cardiac Arrest Patients
February 5, 2019 updated by: Brian O'Neil, Wayne State University
This is an observational study to define the role and future applications of cerebral oximetry in cardiac arrest patients.
Study Overview
Status
Unknown
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
500
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Brian J O'Neil, MD
- Phone Number: 3139932530
- Email: boneil@med.wayne.edu
Study Contact Backup
- Name: Patrick B Medado
- Phone Number: 3135777500
- Email: pbmedado@med.wayne.edu
Study Locations
-
-
Michigan
-
Detroit, Michigan, United States, 48201
- Recruiting
- DMC Detroit Receiving Hospital - Wayne State University
-
Principal Investigator:
- Brian J O'Neil, MD
-
Contact:
- Brian J O'Neil, MD
- Phone Number: 313-993-2530
- Email: boneil@med.wayne.edu
-
Detroit, Michigan, United States, 48235
- Recruiting
- DMC Sinai-Grace Hospital
-
Principal Investigator:
- Brian J O'Neil, MD
-
Contact:
- Thomas Mazzocco, RN
- Phone Number: 313-993-2530
- Email: tmazzocco@med.wayne.edu
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients presenting to the Emergency Department experiencing non-traumatic cardiac arrest or arriving post non-traumatic cardiac arrest
Description
Inclusion Criteria:
- Age > 18 years
- Non-traumatic cardiac arrest or post non-traumatic cardiac arrest
- No purposeful response to verbal or noxious stimuli
Exclusion Criteria:
- Age < 18 years
- Open head injury/trauma
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
CPR Group
|
Non invasive, near infrared spectroscopy cerebral oximetry
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
ROSC
Time Frame: During ED resuscitation
|
Return of spontaneous circulation
|
During ED resuscitation
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
May 1, 2009
Primary Completion (Anticipated)
December 31, 2019
Study Completion (Anticipated)
December 31, 2019
Study Registration Dates
First Submitted
November 8, 2018
First Submitted That Met QC Criteria
December 6, 2018
First Posted (Actual)
December 7, 2018
Study Record Updates
Last Update Posted (Actual)
February 7, 2019
Last Update Submitted That Met QC Criteria
February 5, 2019
Last Verified
February 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 047609MP4E
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
Yes
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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