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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00696722
Other study ID # DM2ATV
Secondary ID 2006.00.055
Status Completed
Phase Phase 2
First received June 11, 2008
Last updated January 24, 2010
Start date June 2008
Est. completion date March 2009

Study information

Verified date January 2009
Source Radboud University
Contact n/a
Is FDA regulated No
Health authority Netherlands: The Central Committee on Research Involving Human Subjects (CCMO)
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether atazanavir use is of influence on the endothelial dysfunction associated with type 2 diabetes mellitus.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date March 2009
Est. primary completion date March 2009
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria (most important):

- 18 - 70 years

- type 2 diabetes mellitus treated with diet, oral medication and/or insulin

- BMI of 18 to 35

- determinants of renal and hepatic function within twice the upper limit of normal range, abnormalities in lipid profile permitted

Exclusion Criteria (most important):

- history of smoking within past year

- history of or current abuse of drugs, alcohol or solvents

- current use of antihypertensive, cardiac or other vasoactive medication

- clinical evidence of cardiac or pulmonary disease

Study Design

Allocation: Randomized, Endpoint Classification: Pharmacodynamics Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
placebo + atazanavir
Placebo treatment first, atazanavir treatment second 4 day treatment
atazanavir + placebo
Atazanavir treatment first, placebo treatment second 4 day treatment

Locations

Country Name City State
Netherlands Radboud University Nijmegen Medical Centre Nijmegen Gelderland

Sponsors (2)

Lead Sponsor Collaborator
Radboud University Dutch Diabetes Research Foundation

Country where clinical trial is conducted

Netherlands, 

Outcome

Type Measure Description Time frame Safety issue
Primary Acetylcholine induced vasodilation following a 4 day treatment with either placebo or atazanavir No
Secondary heme oxygenase expression and activity following a 4 day treatment with either placebo or atazanavir No
Secondary assessment of vascular inflammation by determination of adhesion molecule levels following a 4 day treatment with either placebo or atazanavir No