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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT02238093
Other study ID # 106-13-HYMC
Secondary ID
Status Not yet recruiting
Phase N/A
First received September 10, 2014
Last updated September 10, 2014
Start date October 2014
Est. completion date February 2015

Study information

Verified date September 2014
Source Hillel Yaffe Medical Center
Contact Noa Berar-Yanay, MD
Phone 972-4-630-4115
Email noab@hy.health.gov.il
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Observational

Clinical Trial Summary

Cardiorenal Syndrome (CRS) is prevalent among end-stage renal disease (ESRD) patients. Recently, its prevalence is rising. There are several different clinical presentations of this syndrome. It has a high rate of morbidity and mortality.

The purpose of this study is to find the connection between the heart pathology and its effect on ESRD patients. This will aid in choosing the appropriate medical therapy for these patients, and hopefully, aid in increasing their quality of life, and decrease their morbidity and mortality.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 270
Est. completion date February 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- End-stage renal patients

Exclusion Criteria:

- Cancer patients

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective


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 Heart Pathology Identification Visual identification of heart pathology in ESRD patients using echocardiography by measuring the ejection fraction of the left-ventricle during the systolic and diastolic phases. Valvular pathology is measured by the size of the valve. One hour No
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