- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02725151
Acute Heart Failure Monitoring Via Inferior Vena Cava Ultrasound
February 28, 2021 updated by: Adnan Yamanoğlu, Haseki Training and Research Hospital
The Role of Inferior Vena Cava in Emergency Treatment of Acute Decompensated Heart Failure and Deciding Hospitalization
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.
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
64
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Istanbul, Turkey, 34096
- Adnan Yamanoğlu
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients constitute the study population that was admitted to emergency department with complaint of dyspnea.These patients will be accepted for this study, that known Heart Failure and must be taken diuretic therapy because of volume overload.
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Vena cava inferior diameter change end of each 500cc urination
Time Frame: Maximum 3 hours
|
Maximum 3 hours
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Vena cava inferior diameter change with classic treatment at each hour
Time Frame: Maximum 3 hours
|
Maximum 3 hours
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: Adnan Yamanoğlu, MD, Haseki Training and Research Hospital, Emergency Department
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2015
Primary Completion (Actual)
August 1, 2016
Study Completion (Actual)
January 1, 2017
Study Registration Dates
First Submitted
March 20, 2016
First Submitted That Met QC Criteria
March 30, 2016
First Posted (Estimate)
March 31, 2016
Study Record Updates
Last Update Posted (Actual)
March 2, 2021
Last Update Submitted That Met QC Criteria
February 28, 2021
Last Verified
February 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 231
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
Already in the nearest congress will be shared as an oral presentation or poster
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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