- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02383836
Influence of Position on Detection of Patent Foramen Ovale by Simultaneous Transesophageal Echo and Transcranial Doppler
March 3, 2015 updated by: Hillel Yaffe Medical Center
Patients will have simultaneous Transesophageal Echo (TEE) and Transcranial Doppler (TCD) performed and a comparison of timing, sensitivity and intensity of intravenously injected bubbles will be determined.
Study Overview
Status
Unknown
Conditions
Study Type
Observational
Enrollment (Anticipated)
100
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: David S Blondheim, MD
- Phone Number: 972-463-04488
- Email: davidb@hy.health.gov.il
Study Locations
-
-
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Hadera, Israel, 38100
- Hillel Yaffe Medical Center
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Contact:
- David S Blondheim, MD
- Phone Number: 972-4-630-4488
- Email: davidb@hy.health.gov.il
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Principal Investigator:
- David S Blondheim, MD
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Sub-Investigator:
- Sergiu Shabbtai, MD
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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 and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients referred for a TEE with bubble injection to rule out a cardiac source of brain emboli following an acute neurological embolic event.
Description
Inclusion Criteria:
- Patients needing a TEE evaluation to rule out a cardiac source of brain emboli
Exclusion Criteria:
- Patients unable to comply with protocol requirements
- Patients unable or unwilling to sign informed consent
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Bubble Detection
Time Frame: 3 minutes
|
The amount of time until bubbles are detected will be measured
|
3 minutes
|
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
March 1, 2015
Primary Completion (Anticipated)
March 1, 2016
Study Completion (Anticipated)
August 1, 2016
Study Registration Dates
First Submitted
February 23, 2015
First Submitted That Met QC Criteria
March 3, 2015
First Posted (Estimate)
March 9, 2015
Study Record Updates
Last Update Posted (Estimate)
March 9, 2015
Last Update Submitted That Met QC Criteria
March 3, 2015
Last Verified
March 1, 2015
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 0005-X14-HYMC
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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