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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02649777
Other study ID # 15-2091
Secondary ID UL1TR001082
Status Completed
Phase N/A
First received January 4, 2016
Last updated January 17, 2018
Start date January 2016
Est. completion date December 2017

Study information

Verified date January 2018
Source University of Colorado, Denver
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The role of oxidative stress in disease pathology is increasingly recognized. At present, the development of biomarkers of this state is in its infancy and the availability of clinically validated assays is lacking. This study will better determine normal values for specific biomarkers of oxidative stress. It will also investigate normal values of taurine, a natural occurring oxidative stress protectant. A primary and specific application of this data is for the evaluation of oxidative stress, levels of the natural protectant taurine, and of associated inflammation in the context of cystathionine β-synthase (ClinicalTrials.gov study: Oxidative Stress Markers in Inherited Homocystinuria and the Impact of Taurine).


Description:

This study is a one-time collection of blood and urine samples in healthy individuals. Subjects have to be fasting for 3 hours prior to the blood sampling. A maximum of 7.5 mLs of blood (1 and 1/5 teaspoon) and a urine sample will be collected.


Recruitment information / eligibility

Status Completed
Enrollment 22
Est. completion date December 2017
Est. primary completion date June 2016
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 8 Years to 50 Years
Eligibility Inclusion Criteria:

- Age: Over 8 years old and less than 50 years

Exclusion Criteria:

- Pregnancy: Females who are pregnant or lactating will be excluded from the study as the influence of pregnancy on the markers is not known nor is the impact of pregnancy on taurine known.

- Antioxidant use: Individuals taking taurine, over the counter energy drinks containing taurine or other high dose antioxidants such as Vitamin C or E, coenzyme Q, carotenes, selenium will be excluded as such intake will likely impact laboratory results.

- Inflammatory status:

- Individuals who have a significant chronic illness or state that has a known or suspected marked inflammatory component or oxidative stress component will be excluded from the study as the illness will impact inflammatory markers.

- Patients with an acute illness, which may impact inflammatory biomarkers, will be postponed for study entry until the acute illness is resolved. Entry into the study at a later day will be offered. The study visit will not be conducted within 3 weeks of the acute illness.

- Smoking within the past 12 months will be excluded.

Study Design


Related Conditions & MeSH terms


Locations

Country Name City State
United States Children's Hospital Colorado Aurora Colorado

Sponsors (1)

Lead Sponsor Collaborator
University of Colorado, Denver

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Oxidative stress marker: TBARS Single Draw for one-time analysis Time 0
Primary Metabolite antioxidant: Taurine Single Draw for one-time analysis Time 0
Secondary Inflammation marker: Supper oxide dismutase (SOD) Single Draw for one-time analysis Time 0
Secondary Inflammation marker: TGFß Single Draw for one-time analysis Time 0
Secondary Inflammation marker: myeloperoxidase Single Draw for one-time analysis time 0
Secondary Metabolites: S-adenosylmethionine and S-adenosylhomocysteine Single Draw for one-time analysis (same units) Time 0
Secondary Vascular function: Thromboxane B2 metabolites Single Draw for one-time analysis (same units) Time 0
Secondary Oxidative stress: dityrosine Single Draw for one-time analysis Time 0
Secondary Inflammation markers: IL1a, IL-1ß, IL10, TNFa Single Draw for one-time analysis; ELISA assay (same units) Time 0
Secondary Inflammation markers: cytokines: IL1a, IL-1ß IL-1ra, IL6, IL8, IL17, MCP-1,MIP-1, MIP1a, MIPß Single Draw for one-time analysis; Luminex assay (same units) Time 0
Secondary Inflammation markers: cytokines: TNFa, IL4, IL10 and IL12 Single Draw for one-time analysis; high sensitivity Luminex assay (same units) Time 0
Secondary Inflammation marker: high sensitivity CRP Single Draw for one-time analysis Time 0
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