Efavirenz Versus Rilpivirine on Vascular Function, Inflammation, and Oxidative Stress
A Randomized Controlled Trial Comparing Efavirenz With Rilpivirine on Changes in Endothelial Function, Inflammatory Markers, and Oxidative Stress in HIV-uninfected Healthy Volunteers
Study Overview
Status
Status
Conditions
Conditions
Intervention / Treatment
Intervention / Treatment
Detailed Description
Study Type
Study Type
Enrollment (Actual)
Enrollment
Phase
Phase
- Phase 4
Contacts and Locations
Study Locations
-
-
Indiana
-
Indianapolis, Indiana, United States, 46202
- Indiana Clinical and Translational Sciences Institute
-
-
Participation Criteria
Eligibility Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- 18 years of age or older
- Negative ELISA for HIV-1 or HIV-2 at screening
- Negative hepatitis B surface antigen at screening
- Negative hepatitis C antibody at screening
- For women of reproductive potential, a negative urine pregnancy test at screening and willingness to use two forms of birth control during the course of the study
- For men who are capable of impregnating a female sexual partner, a willingness to use condoms with spermicidal gel for all sexual contacts during the course of the study
- No documented history of or receipt of medications being used to treat any psychiatric disorder, including (but not limited to) depression, dysthymia, mania, bipolar disease, schizophrenia, or previous suicidal ideation/attempts
- No anticipated changes or additions to other medical therapies during the course of the study
- No documented history of seizure disorder
Exclusion Criteria:
- Inability to provide written, informed consent
- Known allergy/intolerance to rilpivirine, efavirenz, or nitroglycerin
- Absolute neutrophil count < 750cell/mL at screening
- Hemoglobin < 11g/dL at screening
- Platelet count < 100,000/mL at screening
- Estimated creatinine clearance (per Cockcroft-Gault equation) < 55 mL/min at screening
- Liver transaminases (AST or ALT) > 100 IU/mL or total bilirubin > 1.5mg/dL at screening
- Serum glucose > 200mg/dL at screening
- Serum total cholesterol > 190mg/dL at screening
- Breastfeeding at screening or during the course of the study
- Hypotension, defined as SBP < 90mmHg at time of each main study visit before brachial artery ultrasound measurements
- Hypertension, defined as SBP > 160mmHg at time of screening
- Receipt of investigational agents within 30 days of each screening visit or anticipated use during the trial
- Receipt of cytotoxic chemotherapy within 30 days of each screening visit or anticipated use during the trial
- Receipt of systemic glucocorticoids (> 10mg/day of prednisone or the equivalent), inhaled/nasal/topical fluticasone, or anabolic steroids within 30 days of each screening visit or anticipated use during the trial
- Use of sildenafil (Viagra or Silagra), vardenafil (Levitra), or tadalafil (Cialis), within 72 hours (before or after) of brachial artery reactivity testing
- Indwelling vascular catheters within any upper body vessel at time of brachial artery reactivity testing
- Active drug or alcohol use or dependence that, in the opinion of the investigator or study personnel, would interfere with adherence to study requirements
- Acute therapy for serious infection or other serious medical illnesses (in the judgment of the site investigator) requiring systemic treatment and/or hospitalization within 14 days prior to each screening and study visit
- History of migraine headaches
- History of Raynaud's phenomenon
- History of cardiac arrythmias
- History of hypothyroidism or hyperthyroidism that is untreated (defined as a TSH outside the normal range on most recent testing during normal clinical care)
- History of carotid bruits
- History of any tobacco use (cigarette smoking, cigar smoking, chewing tobacco) or nicotine replacement treatments (patch, gum) within 45 days of screening
- Drugs/therapies with significant CYP 450 induction or inhibition potential at screening
- Use of antacids, H2-blockers, or proton pump inhibitors within 30 days of screening or anticipated use of these drugs during the trial
- Any history of injection or illicit drug use
- Presence of fever, defined as an oral or tympanic temperature > 100.3F, at either the Entry or Closeout Visits
- On the PHQ-9 depression questionnaire at screening, a total score of more than 9 or any score over 0 on question 9.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Number of Arms
Arms and Interventions
Participant Group / ArmParticipant Group / Arm |
Intervention / TreatmentIntervention / Treatment |
|---|---|
|
Active Comparator: Efavirenz
Efavirenz 600mg given nightly without food for 30 days
|
600mg orally every evening
Other Names:
|
|
Active Comparator: Rilpivirine
Rilpivirine 25mg given daily with meals for 30 days
|
25mg orally once daily
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Change in Flow-mediated Dilation of the Brachial Artery
Time Frame: Change from baseline to 4 weeks
|
This is a measure of in vivo endothelial function
|
Change from baseline to 4 weeks
|
Secondary Outcome Measures
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Inflammatory Markers
Time Frame: Change from baseline to 4 weeks
|
Change in high sensitivity C-reactive protein levels
|
Change from baseline to 4 weeks
|
|
Endothelial Activation Markers
Time Frame: Change from baseline to 4 weeks
|
Change in soluble vascular cell adhesion molecule-1 levels
|
Change from baseline to 4 weeks
|
|
Oxidative Stress Markers
Time Frame: Change from baseline to 4 weeks
|
Change in F2-isoprostane levels
|
Change from baseline to 4 weeks
|
Collaborators and Investigators
Sponsor
Sponsor
Collaborators
Collaborators
Investigators
Investigators
- Principal Investigator: Samir K Gupta, MD, MS, Indiana University School of Medicine
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Study Start
Primary Completion (Actual)
Primary Completion
Study Completion (Actual)
Study Completion
Study Registration Dates
First Submitted
First Submitted
First Submitted That Met QC Criteria
First Submitted That Met QC Criteria
First Posted (Estimate)
First Posted
Study Record Updates
Last Update Posted (Estimate)
Last Update Posted
Last Update Submitted That Met QC Criteria
Last Update Submitted That Met QC Criteria
Last Verified
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Cardiovascular Diseases
- Molecular Mechanisms of Pharmacological Action
- Anti-Infective Agents
- Antiviral Agents
- Reverse Transcriptase Inhibitors
- Nucleic Acid Synthesis Inhibitors
- Enzyme Inhibitors
- Anti-HIV Agents
- Anti-Retroviral Agents
- Cytochrome P-450 Enzyme Inhibitors
- Cytochrome P-450 Enzyme Inducers
- Cytochrome P-450 CYP3A Inducers
- Cytochrome P-450 CYP2B6 Inducers
- Cytochrome P-450 CYP2C9 Inhibitors
- Cytochrome P-450 CYP2C19 Inhibitors
- Efavirenz
- Rilpivirine
Other Study ID Numbers
Other Study ID Numbers
- TMC278HIV4002
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