- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01483495
Assessing Cerebrovascular Reactivity Based on Cerebral Oximetry: a Pilot Study (DOSI)
Assessing Cerebrovascular Reactivity Based on Cerebral Oximetry
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The researcher can use Diffuse Optical Spectroscopy Imaging, cerebral non-invasive oximetry instrument, to determine cerebrovascular reactivity during surgery procedure. Specifically, the cerebral tissue O2 saturation can measure by Diffuse Optical Spectroscopy Imaging can use for cerebral blood flow in the evaluation of cerebrovascular reactivity.
Adequate brain perfusion is critical not only to supply oxygen and nutrients but also to wash out metabolic end products including CO2. Blood flow depends on perfusion pressure and vascular bed resistance. It is well known that multiple physiological and pathological factors affect cerebral vasculature, and the resistance to blood flow. The cerebrovascular responsiveness to those factors determines how well the brain can maintain and adjust its perfusion.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
California
-
Irvine, California, United States, 92612
- UCI Beckman Laser Institute
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Male or Female 20 years of age and older
- Female non-pregnant
- Subject scheduled for elective surgery under general anesthesia with intubation.
- Subject who is able to give informed consent.
Exclusion Criteria:
- Less than 20 years old of age
- Pregnant woman
- Subjects currently diagnosed with severe hypertension, myocardial ischemic disease, symptomatic valvular disease(s), symptomatic arrhythmia, uncompensated congestive heart failure, intracranial aneurysm.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Diagnostic tool
Diffuse Optical Spectroscopy Imaging Cerebrovascular Reactivity
|
Diffuse Optical Spectroscopy Imaging Cerebrovascular Reactivity
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Brain blood flow
Time Frame: 6 hours
|
Optical Imaging assess of Brain blood flow during surgical procedure
|
6 hours
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Lingzhong Meng, M.D, Anesthesiology Perioperative Care
Study record dates
Study Major Dates
Study Start
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
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
- 20107521
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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