Multi-organ Transit Time Acquisition Using Contrast Ultrasound

NCT ID: NCT05135169

Last Updated: 2025-07-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

16 participants

Study Classification

OBSERVATIONAL

Study Start Date

2022-03-03

Study Completion Date

2025-06-30

Brief Summary

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Echocardiographic contrast will be administered to volunteers for the purpose of measuring transit time through various organs/vascular beds

Detailed Description

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Conditions

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Healthy

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Contrast administration

Definity Suspension for Injection

Intervention Type DRUG

Administration of Definity

Interventions

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Definity Suspension for Injection

Administration of Definity

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* at least 18 years old
* able to give informed consent

Exclusion Criteria

1. Known allergic reaction to Definity ultrasound contrast
2. Pregnancy/Nursing - as assessed/disclosed by the participant
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Vanderbilt University Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Ken Monahan

Assistant Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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VUMC

Nashville, Tennessee, United States

Site Status

Countries

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United States

Other Identifiers

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IRB 212087

Identifier Type: -

Identifier Source: org_study_id

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