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NCT02725151 Clinical Trial

Acute Heart Failure Monitoring Via Inferior Vena Cava Ultrasound

Chronic Heart Failure Clinical Trial

Official title:
The Role of Inferior Vena Cava in Emergency Treatment of Acute Decompensated Heart Failure and Deciding Hospitalization

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT02725151
Other study ID # 231
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 2015
Est. completion date January 2017

Study information
Verified date February 2021
Source Haseki Training and Research Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Known before diagnosed heart failure and used diuretic therapy patients will be admitted in this study.The objective of this work is whether the Inferior Vena Cava Ultrasound can be used for management of Acute Heart failure therapy. And investigators will calculation correlation of extracted urine amount with Inferior Vena Cava diameter change. Researchers will not interfere to standard recommended treatment protocol, researchers will correlated the urine amount and changed vital signs with therapy with Vena cava inferior diameter.

Recruitment information / eligibility
Status Completed
Enrollment 64
Est. completion date January 2017
Est. primary completion date August 2016
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: - Adult patients (> 18 years of age) of both sexes) - Non-trauma patients - Non- pregnant patients - All patients will be accepted for this study, that known Heart Failure and must be taken diuretic therapy because of volume overload Exclusion Criteria: - Cardiac tamponade - Aortic dissection - Patients who had suffered cardiopulmonary arrest or been intubated

Study Design

Related Conditions & MeSH terms

Locations
Country Name City State
Turkey Adnan Yamanoglu Istanbul

Sponsors (1)
Lead Sponsor Collaborator
Haseki Training and Research Hospital

Country where clinical trial is conducted

Turkey, 

Outcome
Type Measure Description Time frame Safety issue
Primary Vena cava inferior diameter change end of each 500cc urination Maximum 3 hours
Secondary Vena cava inferior diameter change with classic treatment at each hour Maximum 3 hours
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