- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00660465
Exploring the Relationship Between Varying CO2 Levels and the Regional BOLD Signal, by Using Breathing Exercises
November 9, 2014 updated by: Soroka University Medical Center
Exploring the Relationship Between Varying CO2 Levels and the Regional BOLD Signal, by Using Breathing Exercises .
The purpose of this study is to explore how arterial PaCO2 effect regional Blood Oxygen Level Dependent (BOLD) signal, and indirectly the brain regional O2 level .
Study Overview
Status
Unknown
Conditions
Detailed Description
Among many parameters effecting cerebral blood flow(CBF), partial pressure of CO2 (PaCO2) in arterial blood has a significant effect.
A small increase in arterial PaCO2 level will cause a significant increase of CBF , followed by increase of O2 level .
The main objective is to explore the effect of arterial PaCO2 level on regional CBF and brain O2 level, by using breathing exercises to modulate arterial PaCO2.
The regional Blood Oxygen Level Dependent (BOLD) signal produced by MRI , will indicate the regional O2 level.
Study Type
Observational
Enrollment (Anticipated)
6
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Beer Sheva, Israel, 84101
- Department of Diagnostic Imaging ;Soroka Univrsity Medical Center
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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 to 75 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
residents
Description
Inclusion Criteria:
- adults over 18 years old .
Exclusion Criteria:
- under 18 years old.
- Artificial pacemaker
- implantable cardioverter-defibrillator (ICD)
- Hearing aid, implantable or portable.
- artificial heart valve
- Surgical clips
- Metal fragments in eyes
- Electronic stimulators
- Implanted pumps
- Implantable Neurostimulation Device
- metal fragments of any sort
- Permanent makeup or tattoo
- transfusion pump
- pregnant or breast feeding women
- False teeth , retainer or dental crown
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 |
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A18
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Director: Ilan Shelef, M.D, Head, Neuroradiolgy Unit ;Department of Diagnostic Imaging ;Soroka Univrsity Medical Center
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
May 1, 2008
Study Registration Dates
First Submitted
April 15, 2008
First Submitted That Met QC Criteria
April 16, 2008
First Posted (Estimate)
April 17, 2008
Study Record Updates
Last Update Posted (Estimate)
November 11, 2014
Last Update Submitted That Met QC Criteria
November 9, 2014
Last Verified
February 1, 2008
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- SOR467608CTIL
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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