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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT04336995
Other study ID # IRB200429
Secondary ID
Status Completed
Phase Phase 4
First received
Last updated
Start date August 27, 2020
Est. completion date March 1, 2024

Study information

Verified date April 2024
Source Vanderbilt University Medical Center
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study seeks to measure pulmonary transit time via contrast-echocardiography before and after exercise.


Description:

The ability to measure the amount of blood in the lungs using heart-ultrasound (echocardiography) can be useful to estimate how much fluid is in a patient's circulation, which can influence diagnosis and treatment of certain types of heart failure. In some patients, the amount of fluid is normal at rest, but can increase with activity and thus a diagnosis of heart failure can only be made after exercising. Currently, the amount of fluid is measured invasively. We have shown that echocardiography can measure the amount of fluid in the lung circulation at rest without the need for an invasive procedure. We now seek to find out if we can make a similar measurement after exercise. If successful, the need for catheter procedures may be reduced in certain types of heart failure.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date March 1, 2024
Est. primary completion date August 25, 2021
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Age = 18 years old 2. Able to give informed consent Exclusion Criteria: 1. Known allergic reaction to Definity or Optison ultrasound contrast 2. Pregnancy/Nursing - as assessed/disclosed by the participant

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
contrast echocardiography
giving echocardiographic contrast and taking echocardiographic images before and after exercise

Locations

Country Name City State
United States VHVI Nashville Tennessee

Sponsors (1)

Lead Sponsor Collaborator
Vanderbilt University Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pulmonary Transit Time interval required for the pulmonary blood volume to traverse the pulmonary circulation 3-10 seconds
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