- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT01551836
At What Time Therapeutic Plasma Concentrations of Paracetamol Are Achieved in Two Marketed Formulations
8. mars 2012 oppdatert av: GlaxoSmithKline
A Randomised, Two Way Crossover Study to Determine the Time at Which Therapeutic Plasma Concentrations of Paracetamol Are Achieved in Two Marketed Formulations
This will be a single centre, open label, randomised, two-way crossover study in healthy volunteers under semi-fed conditions.
Two formulations of paracetamol, are being tested in this study to establish at what time point a therapeutic concentration of paracetamol in the blood is reached.
Subjects will attend a screening visit to check if they are eligible for study participation then within 15 days they will check-in to the unit for a stay of approximately 48 hours (hrs).
They will be given a single dose of one of the preparations on the first day and then the other preparation on the next day.
Regular blood samples will be taken along with other assessments for safety.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
12
Fase
- Fase 1
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
-
-
N Ireland
-
Belfast, N Ireland, Storbritannia, BT9 6AD
- GSK Investigational Site
-
-
Deltakelseskriterier
Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
18 år til 55 år (Voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Mann
Beskrivelse
Inclusion Criteria:
- Males in good general heatlh and Body Mass Index between 19-28 kg/m2
Exclusion Criteria:
Disease
- Current liver impairment, renal impairment, history of or active gastrointestinal ulcers, uncontrolled hypertension, haemophilia or other bleeding disorders.
- Current or recurrent disease, within 12 months of the screening, that could affect the action, absorption or disposition of the study formulations or clinical or laboratory assessments (e.g. hepatic disorders, renal insufficiency, congestive heart failure).
- Current or relevant previous history, within 12 months of the screening visit, of serious, severe or unstable physical or psychiatric illness, any medical disorder that may require treatment or make the subject unlikely to fully complete the study, or any condition that presents undue risk from the study treatments or procedures.
Medications
- Current or regular use at screening of any prescription, herbal or Over the Counter (OTC) medication including paracetamol, aspirin, metaclopramide, domperidone, cholestyramine, angiotensin -converting enzyme (ACE) inhibitors, acetazolamide, anticonvulsants, diuretics, methotrexate, non-steroidal anti-inflammatory drugs (NSAIDs) and oral hypoglycemics within the past 48 hrs and monoamine oxidase inhibitors, tricyclic antidepressants, beta blockers and anticoagulants such as warfarin and heparin within the past 2 weeks.
- Subjects who have taken any drug known to induce or inhibit hepatic drug metabolism in the 30 days prior to the screening visit (some examples of inducers: barbiturates, theophylline; inhibitors: cimetidine, erythromycin).
- Subjects for whom the use of any of the study drugs is contraindicated.
- Virology Screening Positive screening for serum Hepatitis B surface antigen, Hepatitis C antibodies or human immunodeficiency virus (HIV).
Drug Screen
- Positive urine screen for drugs of abuse at screening and/or Day-1.
- Positive alcohol breath test on Day-1.
Smoking
- Smoking more than five cigarettes a day.
- Prior (within 7 days of dosing on Day 1) or current use of any other nicotine containing products, other than cigarettes/pipes/cigars.
- Blood donation Has donated blood or plasma or any other blood product within 3 months of the screening visit. Subjects for whom participation in this study would result in having donated more than 1500 ml of blood within the previous 12 months.
Nutrition
- Is a vegetarian or is under a sodium restricted diet.
- Has consumed poppy seed containing foods within 3 days prior to the screening visit and admission on Day -1.
- Has consumed food and beverages containing grapefruit, Seville oranges or marmalade within 24 hrs prior to admission on Day -1.
- Has consumed caffeine containing drinks or food (e.g. tea, coffee, chocolate and cola) 24 hrs prior to admission on Day -1.
- Has consumed alcohol 36 hrs prior to admission on Day -1.
- Has undertaken any unusually strenuous physical activity 24 hrs prior to the screening visit or check-in on Day 1.
- Weight Weight below 50 kg.
- Haemoglobin Subjects with haemoglobin level below 12.0 gram /decilitre (dl).
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Enkelt
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
|
Annen: Paracetamol formulation 1
Higher dose level of marketed paracetamol (compared to the other dosage arm)
|
formulation 1
|
|
Annen: Paracetamol formulation 2
Lower paracetamol concentrations
|
Formulation 2
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Mean time to therapeutic levels of plasma concentration
Tidsramme: within a single day
|
within a single day
|
Sekundære resultatmål
Resultatmål |
Tidsramme |
|---|---|
|
Mean plasma concentrations
Tidsramme: within a single day
|
within a single day
|
Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Studierekorddatoer
Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.
Studer hoveddatoer
Studiestart
1. juni 2009
Primær fullføring (Faktiske)
1. juni 2009
Studiet fullført (Faktiske)
1. juni 2009
Datoer for studieregistrering
Først innsendt
23. juni 2011
Først innsendt som oppfylte QC-kriteriene
8. mars 2012
Først lagt ut (Anslag)
13. mars 2012
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
13. mars 2012
Siste oppdatering sendt inn som oppfylte QC-kriteriene
8. mars 2012
Sist bekreftet
1. mars 2012
Mer informasjon
Begreper knyttet til denne studien
Nøkkelord
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- E3870651
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