- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00631553
Assessment of Changes in Renal Cortical and Medullary Blood Flow by Contrast Ultrasound
August 6, 2008 updated by: University of Virginia
The purpose of this study is to determine if contrast enhanced ultrasound (CEU) using microbubbles, is useful in assessing changes in kidney blood flow.
Study Overview
Study Type
Interventional
Enrollment (Anticipated)
20
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Kambiz Kalantarinia, MD
- Phone Number: 434 924 5125
- Email: kk6c@virginia.edu
Study Contact Backup
- Name: Lori Ratliff, RN ANP
- Phone Number: 4-1572 434 924 5820
- Email: lbr@virginia.edu
Study Locations
-
-
Virginia
-
Charlottesville, Virginia, United States, 22908
- Recruiting
- University of Virginia Health System
-
Principal Investigator:
- Kambiz Kalantarinia, MD
-
Contact:
- Kalantarinia
- Email: kk6cQ@virginia.edu
-
Contact:
- Ratliff
- Email: lbr@virgina.edu
-
-
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
18 years to 65 years (Adult, Older Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Healthy adults
- Males and females
- Ages 18-65 years old
Exclusion Criteria:
- Pregnancy or lactation
- H/o kidney disease
- H/o congestive heart failure, ischemic heart disease, severe pulmonary disease or allergy to the drug
- H/o any cardiovascular disease
- Abnormal liver function (liver function tests out of specified ranges)
- Screening urinalysis which indicates infection or inflammation
- Taking regular medications (except for over-the-counter vitamins or hormonal contraceptives.)
- Taking supplements, like protein shakes
- Unwilling or unable to eat chicken (used as protein meal)
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
- Primary Purpose: Diagnostic
- Allocation: N/A
- Interventional Model: Single Group Assignment
- Masking: None (Open Label)
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
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
June 1, 2006
Study Completion (Anticipated)
December 1, 2009
Study Registration Dates
First Submitted
February 27, 2008
First Submitted That Met QC Criteria
March 6, 2008
First Posted (Estimate)
March 7, 2008
Study Record Updates
Last Update Posted (Estimate)
August 7, 2008
Last Update Submitted That Met QC Criteria
August 6, 2008
Last Verified
August 1, 2008
More Information
Terms related to this study
Other Study ID Numbers
- 12014 (DAIDS-ES Registry Number)
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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