Pharmacokinetics of Antiretroviral Agents in HIV-infected Pregnant Women.
A legfontosabb adatok
- Hol
- Brussels (Belgium)A helyszín megnézése
Helyszínek itt: Belgium
- Saint-Pierre University Hospital; Department of Infectious DiseasesBrussels, BelgiumContact: D KonopnickiRésztvevőt keres
Kérdések a vizsgálat csapatának
- Milyen gyakran kell bejárnom, és egy-egy alkalom mennyi ideig tart?
- Megtérítik az utazási költséget?
- Megtarthatom a saját orvosomat?
- Mi történik, ha ki akarok lépni?
Contact the study team: see the registry record → Contacts and Locations
Oldal nyomtatása az orvosomnakA vizsgálat adatai
- Ki végzi
- Radboud University Medical Center
- Azonosító
- NCT00825929
- A regiszteradat frissítve
- 2025. január 13.
- Eredeti leírás
Due to the potential for pregnancy-induced changes in the pharmacokinetics of medication, one cannot assume that the currently licensed doses of the medication to be tested under this protocol lead to adequate exposure in an HIV-infected pregnant woman. For the agents under study no or limited pharmacokinetic data during pregnancy are available. As the changes in pharmacokinetics during pregnancy are most prominent in the third trimester a pharmacokinetic curve will be recorded in the third trimester after attaining steady state.A teljes eredeti leírásKevesebb
Study on Pharmacokinetics of Newly Developed ANtiretroviral Agents in HIV-infected pregNAnt Women (PANNA)
Due to the potential for pregnancy-induced changes in the pharmacokinetics of medication, one cannot assume that the currently licensed doses of the medication to be tested under this protocol lead to adequate exposure in an HIV-infected pregnant woman. For the agents under study no or limited pharmacokinetic data during pregnancy are available. As the changes in pharmacokinetics during pregnancy are most prominent in the third trimester a pharmacokinetic curve will be recorded in the third trimester after attaining steady state.
Bevonási feltételek: HIV-infected as documented by positive HIV antibody test and confirmed by an antigen test; Subject is at least 18 years of age at screening; Subject is able and willing to sign the Informed Consent Form prior to screening evaluations; Treated with a cART regimen containing at least one agent which is mentioned in Appendix 1; this agent has been taken for at least 2 weeks before the day of first PK curve evaluation; Subject is pregnant; Subject is able to adhere to food intake recommendations, if applicable.
Kizáró feltételek: Relevant history or current condition that might interfere with drug absorption, distribution, metabolism or excretion; Presence of grade III/IV anemia (i.e. Hb <4.6 mmol/L or <7.4 g/dL); Inability to understand the nature and extent of the study and the procedures required; Using oral cabotegravir/rilpivirine.