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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00616707
Other study ID # 200614513
Secondary ID
Status Completed
Phase N/A
First received February 4, 2008
Last updated May 25, 2017
Start date August 2006
Est. completion date October 2009

Study information

Verified date May 2017
Source University of California, Davis
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine if there are signs of inflammation in one's blood and urine and to find out if one's body size or ethnicity has an effect on these substances.


Recruitment information / eligibility

Status Completed
Enrollment 68
Est. completion date October 2009
Est. primary completion date October 2009
Accepts healthy volunteers No
Gender All
Age group 12 Years to 18 Years
Eligibility Inclusion Criteria:

- Adolescents between 12 to 18 years old

- Hispanic, African American or Caucasian ethnicity

- Have a Body Mass Index (BMI) between the 5th and 85th percentile or greater than the 95th percentile

- Must currently be attending a UC Davis Pediatric clinic

Exclusion Criteria:

- Chronic liver or kidney disease, known Diabetes or other chronic illnesses (such as Sickle Cell Disease or Cystic Fibrosis)

- Subjects can NOT be acutely febrile, smoke, chronically use prescription medications or oral contraceptive pills.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States UC Davis Medical Center Sacramento California

Sponsors (2)

Lead Sponsor Collaborator
University of California, Davis Children's Miracle Network

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To compare plasma levels of inflammatory markers and urinary biomarkers of oxidative stress in adolescents of Hispanic, African-American and Caucasian ethnicity at the end of study
Secondary To determine if there is an independent correlation between these markers and urinary microalbumin excretion at the end of study
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