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
Studieoversigt
Status
Status
Betingelser
Betingelser
Intervention / Behandling
Intervention / Behandling
Detaljeret beskrivelse
Undersøgelsestype
Undersøgelsestype
Tilmelding (Faktiske)
Tilmelding
Fase
Fase
- Fase 4
Kontakter og lokationer
Studiesteder
-
-
Indiana
-
Indianapolis, Indiana, Forenede Stater, 46202
- Indiana Clinical and Translational Sciences Institute
-
-
Deltagelseskriterier
Berettigelseskriterier
Berettigelseskriterier
Aldre berettiget til at studere
Tager imod sunde frivillige
Køn, der er berettiget til at studere
Beskrivelse
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.
Studieplan
Hvordan er undersøgelsen tilrettelagt?
Design detaljer
- Primært formål: Behandling
- Tildeling: Randomiseret
- Interventionel model: Parallel tildeling
- Maskning: Enkelt
Antal våben
Våben og indgreb
Deltagergruppe / ArmDeltagergruppe / Arm |
Intervention / BehandlingIntervention / Behandling |
|---|---|
|
Aktiv komparator: Efavirenz
Efavirenz 600mg given nightly without food for 30 days
|
600mg orally every evening
Andre navne:
|
|
Aktiv komparator: Rilpivirine
Rilpivirine 25mg given daily with meals for 30 days
|
25mg orally once daily
Andre navne:
|
Hvad måler undersøgelsen?
Primære resultatmål
Primære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Change in Flow-mediated Dilation of the Brachial Artery
Tidsramme: Change from baseline to 4 weeks
|
This is a measure of in vivo endothelial function
|
Change from baseline to 4 weeks
|
Sekundære resultatmål
Sekundære resultatmål
Resultatmål |
Foranstaltningsbeskrivelse |
Tidsramme |
|---|---|---|
|
Inflammatory Markers
Tidsramme: Change from baseline to 4 weeks
|
Change in high sensitivity C-reactive protein levels
|
Change from baseline to 4 weeks
|
|
Endothelial Activation Markers
Tidsramme: Change from baseline to 4 weeks
|
Change in soluble vascular cell adhesion molecule-1 levels
|
Change from baseline to 4 weeks
|
|
Oxidative Stress Markers
Tidsramme: Change from baseline to 4 weeks
|
Change in F2-isoprostane levels
|
Change from baseline to 4 weeks
|
Samarbejdspartnere og efterforskere
Sponsor
Sponsor
Samarbejdspartnere
Samarbejdspartnere
Efterforskere
Efterforskere
- Ledende efterforsker: Samir K Gupta, MD, MS, Indiana University School of Medicine
Publikationer og nyttige links
Datoer for undersøgelser
Studer store datoer
Studiestart
Studiestart
Primær færdiggørelse (Faktiske)
Primær færdiggørelse
Studieafslutning (Faktiske)
Studieafslutning
Datoer for studieregistrering
Først indsendt
Først indsendt
Først indsendt, der opfyldte QC-kriterier
Først indsendt, der opfyldte QC-kriterier
Først opslået (Skøn)
Først opslået
Opdateringer af undersøgelsesjournaler
Sidste opdatering sendt (Skøn)
Sidste opdatering sendt
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier
Sidst verificeret
Sidst verificeret
Mere information
Begreber relateret til denne undersøgelse
Nøgleord
Yderligere relevante MeSH-vilkår
- Hjerte-kar-sygdomme
- Molekylære mekanismer for farmakologisk virkning
- Anti-infektionsmidler
- Antivirale midler
- Reverse transkriptasehæmmere
- Nukleinsyresyntesehæmmere
- Enzymhæmmere
- Anti-HIV-midler
- Anti-retrovirale midler
- Cytokrom P-450 enzymhæmmere
- Cytokrom P-450 enzyminducere
- Cytokrom P-450 CYP3A inducere
- Cytokrom P-450 CYP2B6 inducere
- Cytokrom P-450 CYP2C9-hæmmere
- Cytokrom P-450 CYP2C19-hæmmere
- Efavirenz
- Rilpivirin
Andre undersøgelses-id-numre
Andre undersøgelses-id-numre
- TMC278HIV4002
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