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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT01264159
Other study ID # 0090-10-HYMC
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date January 1, 2011
Est. completion date July 1, 2015

Study information

Verified date June 2020
Source Hillel Yaffe Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It is well known that 20-25% of patients hospitalized for acute myocardial infarction will develop acute heart failure during their hospitalization. Currently, the investigators have no reliable parameter for prediction of evolving acute heart failure in such a group of patients. As a result, the investigators have no way of preventing acute heart failure. Treatment of these patients only begins after appearance of clinical signs of acute heart failure. Lung impedance monitoring may be a good non-invasive parameter for prediction of evolving acute heart failure. This study will attempt to address whether preemptive lung impedence-guided therapy may prevent the development of overt acute heart failure and improve their clinical outcome.


Recruitment information / eligibility

Status Terminated
Enrollment 70
Est. completion date July 1, 2015
Est. primary completion date January 1, 2015
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Patients hospitalized in the ICCU for acute myocardial infarction and developing acute heart failure during their hospitalization

Exclusion Criteria:

- Patients with acute myocardial infarction with clinical and radiological signs of acute heart failure at admission

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Lung impedence-guided therapy

Other:
Usual treatment of patients with developing acute heart failure


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 Prevention of acute heart failure development in acute MI patients Three years
Secondary Improvement of clinical outcome in patients with lung impedence-guided treatments Three years
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