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NCT01296282 Clinical Trial

Comparison Between Internal and External Chest Impedance Measurement

Heart Failure Clinical Trial

Clinical Trial Details — Status: Not yet recruiting

Administrative data
NCT number NCT01296282
Other study ID # 0094-10-HYMC
Secondary ID
Status Not yet recruiting
Phase N/A
First received February 13, 2011
Last updated February 13, 2011
Start date March 2011
Est. completion date April 2015

Study information
Verified date February 2011
Source Hillel Yaffe Medical Center
Contact Mark Kazatsker, MD
Phone 972-4-630-4656
Email markk@hy.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

To compare two methods of chest impedance: the Medtronics Optivol Measurement via CRT pacemakers for patients with heart failure and external non-invasive measurement

Recruitment information / eligibility
Status Not yet recruiting
Enrollment 50
Est. completion date April 2015
Est. primary completion date April 2015
Accepts healthy volunteers No
Gender Both
Age group N/A and older
Eligibility Inclusion Criteria:

- CRT-implanted patients with heart failure

Exclusion Criteria:

- All others

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Intervention

Device:
• Medronics CRT Optivol Impedance Measurement
Pacemaker
• External Thoracic Impedance Measurement

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 External measurement of chest impedance can be effective in monitoring heart failure patients Three years No
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