- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04510363
Optic Nerve Sheath Diameter, Carotid Duplex and Transcranial Duplex as a Prognostic Factor
Optic Nerve Sheath Diameter, Carotid Duplex and Transcranial Duplex as a Prognostic Predicting Factor in Post-cardiac Arrest Patients
Study Overview
Status
Conditions
Detailed Description
Prediction of the neurological outcome in resuscitated post-cardiac arrest patients is important to tailor appropriate management plans. Brain imaging, electrophysiological evaluations, biomarkers all take part in neuroprognosis in cardiac arrest patients, however, these modalities are more expensive or not suitable to repeat in a short time. Optic nerve sheath diameter (ONSD) had been proved to be associated with increased intracranial pressure2 and can be used as one of the prognostic factors in cardiac arrest patients. It is simple, quick and can be measured repeatedly. Carotid duplex and transcranial duplex(TCD) provide rapid, noninvasive, real-time measures of cerebrovascular function. It can be used to assess the vascular territory by measuring blood flow, and to evaluate factors include brain perfusion, plaque morphology, and patency of intracranial collaterals.
Hence, it could act as a crucial role in neuroprognosis in post-arrest patients. In this study, the investigator aimed to analyze the ONSD diameters, ONSD/ETD ratio, carotid duplex and transcaranial duplex parameters in different stages of post-cardiac arrest care, demographic characteristics and resuscitation information with the neurological outcome of post-cardiac arrest patients.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Wan-Ching Lien, PhD
- Phone Number: 65655 +886-223123456
- Email: wanchinglien@ntu.edu.tw
Study Locations
-
-
-
Taipei, Taiwan, 100
- Recruiting
- National Taiwan University Hospital
-
Contact:
- Wan-Ching Lien, MD., PhD
- Phone Number: 65637 +886-2-23123456
- Email: wanchinglien@ntu.edu.tw
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
. Non-traumatic cardiac arrest adult patients achieving return of spontaneous circulation after resuscitation
Exclusion Criteria:
- traumatic cardiac arrests
- non-traumatic arrest patients without return of spontaneous circulation after resuscitation
Study Plan
How is the study designed?
Design Details
- Observational Models: Case-Control
- Time Perspectives: Prospective
Cohorts and Interventions
Group / Cohort |
|---|
|
cardiac arrest survivors
|
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age- and sex-matched controls
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
optic nerve sheath diameter (ONSD)
Time Frame: 7 days
|
ONSD measured by ultrasonography during the post-arrest care
|
7 days
|
|
carotid artery resistance
Time Frame: 7 days
|
carotid artery resistance measured by ultrasonography during the post-arrest care
|
7 days
|
|
middle cerebral artery resistance
Time Frame: 7 days
|
middle cerebral artery resistance measured by ultrasonography during the post-arrest care
|
7 days
|
Collaborators and Investigators
Investigators
- Principal Investigator: Wan-Ching Lien, PhD, National Taiwan University Hospital
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 201911027RINC
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
product manufactured in and exported from the U.S.
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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