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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00567593
Other study ID # DK59961
Secondary ID R01DK059961
Status Completed
Phase Phase 4
First received December 3, 2007
Last updated April 9, 2014
Start date October 2007
Est. completion date March 2008

Study information

Verified date April 2014
Source University of Pennsylvania
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine the effect of rosiglitazone on the genes of the colon


Description:

The primary aim of the study is to examine the effect of rosiglitazone (Avandia) on gene regulation in colonic epithelium in the absence of pathologic acute and chronic intestinal inflammation. The secondary aims are to determine the effect of rosiglitazone (Avandia) therapy on T cell activation and cytokine expression in the absence of pathologic acute and chronic intestinal inflammation.


Recruitment information / eligibility

Status Completed
Enrollment 12
Est. completion date March 2008
Est. primary completion date March 2008
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- Capable of giving informed consent

- Agrees to use a barrier method of birth control for the duration of the study

Exclusion Criteria:

- History of inflammatory bowel disease

- Has taken prescription or over the counter medications in the two weeks prior to enrollment

- History of diabetes, heart failure, angina, hypertension, coronary heart disease, cancer, bleeding disorder, HIV, AIDS

- Fasting LDL >160 mg/dl

- History of smoking in the year prior to enrollment

- Pregnant or breastfeeding

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Basic Science


Intervention

Drug:
Rosiglitazone
8mg tablet once a day for 14 days

Locations

Country Name City State
United States University of Pennsylvania Clinical and Translational Research Center Philadelphia Pennsylvania

Sponsors (2)

Lead Sponsor Collaborator
James Lewis National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary PDK4 mRNA 14 No
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