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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03447574
Other study ID # 17-007104
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date June 27, 2018
Est. completion date October 26, 2022

Study information

Verified date December 2022
Source Mayo Clinic
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is designed to answer the question of if several non-invasive methods are comparable to the invasive clinical gold standard of radiolabeled albumin in terms of detecting changes in fluid volume. It is broken into two studies: Aim 1 Study A is designed as a pilot phase to develop the non-techniques, and Aim 2 Study B is comparing these techniques to the gold standard.


Recruitment information / eligibility

Status Completed
Enrollment 14
Est. completion date October 26, 2022
Est. primary completion date October 26, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years and older
Eligibility 1. Non-smokers 2. Have a BMI<30 3. Have no chronic disease 4. Be free of medications with known cardiovascular effects

Study Design


Related Conditions & MeSH terms

  • Development of Non-invasive Protocol

Intervention

Other:
ethanol dilution
Ethanol has been validated against deuterium oxide, the invasive gold standard for determining totally body water

Locations

Country Name City State
United States Mayo Clinic in Florida Jacksonville Florida
United States Mayo Clinic in Rochester Rochester Minnesota
United States Mayo Clinic in Arizona Scottsdale Arizona

Sponsors (1)

Lead Sponsor Collaborator
Mayo Clinic

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Validation against Gold Standard The non-invasive methods being investigated will be non-inferior in measuring the blood or fluid volumes in healthy participants when compared to the gold standard. 2 years

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