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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02383836
Other study ID # 0005-X14-HYMC
Secondary ID
Status Not yet recruiting
Phase N/A
First received February 23, 2015
Last updated March 3, 2015
Start date March 2015
Est. completion date August 2016

Study information

Verified date March 2015
Source Hillel Yaffe Medical Center
Contact David S Blondheim, MD
Phone 972-463-04488
Email davidb@hy.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 100
Est. completion date August 2016
Est. primary completion date March 2016
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility 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 Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Israel Hillel Yaffe Medical Center Hadera

Sponsors (1)

Lead Sponsor Collaborator
Hillel Yaffe Medical Center

Country where clinical trial is conducted

Israel, 

Outcome

Type Measure Description Time frame Safety issue
Primary Bubble Detection The amount of time until bubbles are detected will be measured 3 minutes No
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