- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02729857
Postprandial Response After Intake of Meals With Different Fatty Acid Composition
29. juni 2016 oppdatert av: Kirsten Holven, University of Oslo
Postprandial Response After Intake of Meals With Different Fatty Acid Composition in Patients With Familial Hypercholesterolemia and Healthy Subjects
The aim of the study is to understand more about how different fatty acids modulate postprandial lipid metabolism and inflammatory response.
Studieoversikt
Status
Fullført
Forhold
Intervensjon / Behandling
Studietype
Intervensjonell
Registrering (Faktiske)
31
Fase
- Ikke aktuelt
Kontakter og plasseringer
Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.
Studiesteder
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Post box 1046, Blindern
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Oslo, Post box 1046, Blindern, Norge, 0317
- University of Oslo
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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 30 år (Voksen)
Tar imot friske frivillige
Ja
Kjønn som er kvalifisert for studier
Alle
Beskrivelse
Inclusion Criteria:
- 18 - 30 years of age
Healthy or diagnosed with familial hypercholesterolemia (FH) (mutation in gene coding for LDL-receptor). FH subjects can be included if they are:
- Untreated
- Treated with low dose statin (<20 mg atorvastatin, <10-20 mg simvastatin or <5-10 mg rosuvastatin)
- Treated with high dose statin and willing to use low dose statin during the last 4 weeks prior to both study visits (total 8 week period)
- Treated with high dose statins and willing to discontinue statin treatment during the last 4 weeks prior to both study visits (total 8 week period)
- BMI 18.5 - 30 kg/m2
- Stabile weight the last three months prior to the first study visit (weight change less than ± 5 % of body weight)
Exclusion Criteria:
- CRP >10 mg/L
- TG >4 mmol/L
- Comorbidities including diabetes type I and II, coronary heart disease, haemophilia, anaemia, gastro intestinal disease, renal failure and hyperthyroidism
- Pregnant or lactating
- Allergic or intolerant to gluten or egg
- Not willing to stop using n-3 fatty acid supplements during the last 4 weeks prior to both study visits
- Using medications affecting lipid metabolism or inflammation, except statins for FH subjects
- Hormone treatment (except contraception and thyroxin (stabile dose last 3 months))
- Donating blood 2 months within or during study period
- Tobacco smoking
- Large alcohol consumption (>40g daily)
Studieplan
Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Firemannsrom
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
|---|---|
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Eksperimentell: Familial hypercholesterolemia
Subjects diagnosed with familial hypercholesterolemia receive in randomized order muffin with saturated fat (SFA muffin) and polyunsaturated fat (PUFA muffin) at baseline
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Muffin rich in saturated fat.
Muffin rich in polyunsaturated fat.
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Aktiv komparator: Healthy
Subjects with no chronic diseases receive in randomized order muffin with saturated fat (SFA muffin) and polyunsaturated fat (PUFA muffin) at baseline
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Muffin rich in saturated fat.
Muffin rich in polyunsaturated fat.
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Hva måler studien?
Primære resultatmål
Resultatmål |
Tidsramme |
|---|---|
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Change in levels of circulating triglycerides
Tidsramme: Measured at baseline and 2,4 and 6 hours after intake of test meal
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Measured at baseline and 2,4 and 6 hours after intake of test meal
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Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
|---|---|---|
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Changes in markers of lipid- and glucose metabolism
Tidsramme: Measured at baseline and 2,4 and 6 hours after intake of test meal
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Changes in levels of total cholesterol, low-density lipoprotein, high-density lipoprotein, apolipoprotein (apo) B, apo A1, apo CIII, apo B48, lipoprotein (a), free fatty acids, total fatty acid composition, LDL-receptor-related protein with 11 ligand-binding repeats (LR11), HbA1c, glucose, insulin and troponin.
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Measured at baseline and 2,4 and 6 hours after intake of test meal
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Changes in circulating levels of inflammatory markers
Tidsramme: Measured at baseline and 2,4 and 6 hours after intake of test meal
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Changes in levels of inflammatory markers in circulation such as i.e. cytokines and hsCRP
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Measured at baseline and 2,4 and 6 hours after intake of test meal
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Changes in PBMC gene expression levels of markers of inflammation and lipid metabolism
Tidsramme: Measured at baseline and 2, 4 and 6 hours after intake of test meal
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Changes in levels of markers of inflammation and lipid metabolism at PBMC gene expression level
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Measured at baseline and 2, 4 and 6 hours after intake of test meal
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Changes in lipid classes and lipoprotein size
Tidsramme: Measured at baseline and 2,4 and 6 hours after intake of test meal
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Measured at baseline and 2,4 and 6 hours after intake of test meal
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Changes in plasma and urine metabolomics
Tidsramme: Measured in plasma at baseline and 2,4 and 6 hours after intake of test meal. Measured in urine at fasting state and during the 6 hour postprandial phase.
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Changes in metabolites such as glucose, lactate, pyruvate, citrate and amino acids will be measured in plasma and urine.
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Measured in plasma at baseline and 2,4 and 6 hours after intake of test meal. Measured in urine at fasting state and during the 6 hour postprandial phase.
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Check DNA for single nuclear polymorphisms
Tidsramme: Measured at baseline and 2,4 and 6 hours after intake of test meal
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Measured at baseline and 2,4 and 6 hours after intake of test meal
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Changes in PBMC Whole genome transcriptomics
Tidsramme: Measured at baseline and 4 and 6 hours after intake of test meal
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Measured at baseline and 4 and 6 hours after intake of test meal
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Samarbeidspartnere og etterforskere
Det er her du vil finne personer og organisasjoner som er involvert i denne studien.
Sponsor
Etterforskere
- Hovedetterforsker: Kirsten Bjørklund Holven, Professor, Institute of Basic Medical Sciences, Faculty of medicine, University of Oslo
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. mars 2016
Primær fullføring (Faktiske)
1. juni 2016
Studiet fullført (Faktiske)
1. juni 2016
Datoer for studieregistrering
Først innsendt
31. mars 2016
Først innsendt som oppfylte QC-kriteriene
5. april 2016
Først lagt ut (Anslag)
6. april 2016
Oppdateringer av studieposter
Sist oppdatering lagt ut (Anslag)
30. juni 2016
Siste oppdatering sendt inn som oppfylte QC-kriteriene
29. juni 2016
Sist bekreftet
1. juni 2016
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- 2015/2392/REK sør-øst B
Plan for individuelle deltakerdata (IPD)
Planlegger du å dele individuelle deltakerdata (IPD)?
NEI
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .