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Drug Interactions Between Echinacea Purpurea and Darunavir/Ritonavir

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StatusDovršeno
Sponzori
Germans Trias i Pujol Hospital
Suradnici
IrsiCaixa
Fundacio Lluita Contra la SIDA

Ključne riječi

Sažetak

The purpose of this clinical trial is to characterize drug interactions between one medicinal herb widely used by HIV infected patients: Echinacea sp. and the protease inhibitor darunavir/ritonavir.

Opis

15 patients on antiretroviral therapy with darunavir/ritonavir 600/100 mg twice a day during four weeks will be recruited. The patients will receive treatment with Echinacea purpurea for 14 days, 500 mg every 6 hours. A 12 hour pharmacokinetic curve will be obtained at baseline and on day 14.

Datumi

Posljednja provjera: 11/30/2019
Prvo podneseno: 01/10/2010
Predviđena prijava poslana: 01/10/2010
Prvo objavljeno: 01/11/2010
Posljednje ažuriranje poslano: 12/02/2019
Posljednje ažuriranje objavljeno: 12/03/2019
Stvarni datum početka studija: 12/31/2009
Procijenjeni datum primarnog završetka: 02/28/2010
Procijenjeni datum završetka studije: 03/31/2010

Stanje ili bolest

HIV Infections

Intervencija / liječenje

Drug: darunavir/ritonavir + root of Echinacea purpurea

Faza

Faza 4

Grupe ruku

RukaIntervencija / liječenje
Experimental: darunavir/ritonavir + root of Echinacea purpurea
darunavir/ritonavir + root of Echinacea purpurea
Drug: darunavir/ritonavir + root of Echinacea purpurea
darunavir/ritonavir 600/100 mg + root of Echinacea purpurea 500 mg every 6 hours

Kriterij prihvatljivosti

Dobni uvjeti za studiranje 18 Years Do 18 Years
Spolovi koji ispunjavaju uvjete za studijAll
Prihvaća zdrave volontereDa
Kriteriji

Inclusion Criteria:

1. Patients infected with HIV-1 (at least one documented positive Western-Blot).

2. Age =/+ 18 years.

3. Patients receiving antiretroviral therapy containing darunavir / ritonavir at the approved dose of 600/100 mg twice daily for at least 4 weeks

4. HIV viral load in plasma <50 copies / mL

5. Absence of acute infections and / or tumors in the three months prior to inclusion.

6. Subject able to follow the treatment period, without suspicion of poor adherence in previous antiretroviral treatments.

7. Voluntary written informed consent.

Exclusion Criteria:

1. Any clinical or historical observation that could interfere with the pharmacokinetics of medications, such as gastrointestinal illness or surgery (except for herniotomy and appendectomy), changes in the composition of plasma proteins, some indication of hepatic or renal dysfunction.

2. Active alcohol consumption (> 50 g / day) or illicit drugs (except cannabis).

3. Pregnancy or lactation

Ishod

Primarne mjere ishoda

1. plasma concentration of darunavir and ritonavir [DAY 14]

Sekundarne mjere ishoda

1. Clearance (CL/F) [DAY 14]

2. Volume of distribution (V/F) [DAY 14]

3. Elimination half-life (t1/2) [DAY 14]

4. Area under the plasma concentration-time curve during the dosing interval [DAY 14]

5. Adverse events and laboratory alterations [DAY 14]

6. HIV Viral load in plasma [DAY 14]

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