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Effekt og sikkerhed af Berberine i ikke-alkoholisk Steatohepatitis (EASYBEinNASH)

19. september 2026 opdateret af: Xin Gao, Fudan University

Effekt og sikkerhed af berberin i ikke-alkoholisk Steatohepatitis: et multicenter, randomiseret, placebokontrolleret forsøg

The purpose of this study is to evaluate the efficacy and safety of berberine treatment on Non-alcoholic Steatohepatitis.

Studieoversigt

Status

Afsluttet

Betingelser

Intervention / Behandling

Detaljeret beskrivelse

This is a multicenter, double-blinded, randomized, placebo-controlled clinical trial to investigate the efficacy and safety of berberine on subjects with Non-alcoholic Steatohepatitis.Patients with biopsy-proven non-alcoholic steatohepatitis (NASH) from 18-65 years of age were enrolled. Patients should had no excessive alcohol intake or use of any hepatoprotective or hepatotoxicity medication within 3 months before enrollment.Patients will have an screening period 12 weeks, and a 48-week double-blinded treatment period.

Undersøgelsestype

Interventionel

Tilmelding (Faktiske)

89

Fase

  • Fase 2

Kontakter og lokationer

Dette afsnit indeholder kontaktoplysninger for dem, der udfører undersøgelsen, og oplysninger om, hvor denne undersøgelse udføres.

Studiesteder

      • Hangzhou, Kina
        • The Affiliated Hospital of Hangzhou Normal University
      • Shanghai, Kina
        • Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
      • Shanghai, Kina
        • Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
      • Tianjin, Kina
        • Tianjin Third Central Hospital
      • Ürümqi, Kina
        • Xinjiang Medical University
    • Shanghai Municipality
      • Shanghai, Shanghai Municipality, Kina
        • Department of Endocrinology and Metabolism,Shanghai 6th People's Hospital

Deltagelseskriterier

Forskere leder efter personer, der passer til en bestemt beskrivelse, kaldet berettigelseskriterier. Nogle eksempler på disse kriterier er en persons generelle helbredstilstand eller tidligere behandlinger.

Berettigelseskriterier

Aldre berettiget til at studere

18 år til 75 år (Voksen, Ældre voksen)

Tager imod sunde frivillige

Ingen

Køn, der er berettiget til at studere

Alle

Beskrivelse

The inclusion criteria are as follows:

  1. 18-75 years old, no limitation for ethnicity and gender.

  2. BMI is no more than 40 kg/m2.

  3. Patients with NASH based on liver biopsy obtained within 24 weeks before randomization. The histological evidence of NASH is defined as NAS ≥5 [] or NAS ≥4 with a minimum score of 1 for all of three components (steatosis, hepatocyte ballooning, and lobular inflammation), the diagnosis of NASH for EASYBEinNASH eligibility is based on reviews by three pathologists. If there are controversial pathologic diagnosis, at least 2 of the 3 pathologists are consistent with the pathologic diagnosis, which will be the final pathological diagnosis. If there are three different pathological diagnoses, it needs to be discussed and make a judgment by the chief pathologist to form the final pathology report.

  4. For patients with impaired glucose metabolism, one of the three following conditions needs to be met.

    ① For patients diagnosed as impaired glucose regulation, they will be treated with lifestyle intervention without hypoglycemic drugs;

    ② For patients diagnosed as diabetes and treated with hypoglycemic drugs, the treatment regimen should not be changed and the dosage should remain stable for more than 2 months before randomization;

    ③ For patients diagnosed as diabetes and treated with lifestyle intervention without hypoglycemic drugs, the treatment regimen should not be changed before randomization.

  5. All participants agree to sign the informed consent form.

Exclusion criteria

  1. Excessive alcohol intake ( > 140 g per week for men and >70 g per week for women within 6 months before enrollment);
  2. Liver enzymes (ALT or aspartate aminotransferase(AST) is 5 times higher than the upper limit of normal range;
  3. Liver diseases caused by other reasons, such as alcohol abuse, viral hepatitis, drugs, auto-immune hepatitis, hereditary liver disease, liver cirrhosis, liver cancer, etc;
  4. Biliary tract diseases, biliary obstructive disease, etc;
  5. Other diseases that affect glucose and lipid metabolism, such as hypothyroidism, hyperthyroidism, hypercortisolism, etc;
  6. Diabetic patients with poor blood glucose control: HbA1c >9.5%;
  7. Use of drugs that may affect the outcome measures of this study 3 months before enrollment, including pioglitazone, GLP-1 receptor agonist, DPP-4 inhibitor, insulin, and glycyrrhizic acid preparation, etc;
  8. Chronic kidney disease or severe renal impairment, defined as serum creatinine greater than 2.0mg/dL (176.8umol/L);
  9. Life expectancy is no more than 5 years;
  10. Pregnant or planning to become pregnant within the next 64 weeks for female participant;
  11. Any situation that may affect the implementation or results of the study;
  12. Continuous use of drugs that may affect steatohepatitis 3 months before enrollment, such as glucocorticoids, methotrexate, etc;
  13. Subjects participated in other clinical trials in the past 4 weeks; The researchers did not think they were suitable for the study.

Studieplan

Dette afsnit indeholder detaljer om studieplanen, herunder hvordan undersøgelsen er designet, og hvad undersøgelsen måler.

Hvordan er undersøgelsen tilrettelagt?

Design detaljer

  • Primært formål: Behandling
  • Tildeling: Randomiseret
  • Interventionel model: Parallel tildeling
  • Maskning: Firedobbelt

Våben og indgreb

Deltagergruppe / Arm
Intervention / Behandling
Eksperimentel: Berberine

Berberine was taken orally 0.5g three times per day for 48 weeks, based on lifestyle intervention.

Lifestyle intervention is consisted of diet control and aerobic exercise. calorie restriction: to subtract 500 kcal from daily calorie intake aerobic exercise: medium intensity aerobic exercise for more than 150 min per week with heart rate around 50-70% of the maximal heart rate.

Berberine tablets 0.5 tid, 30 minutes before each meal, for 48weeks

Placebo komparator: Placebo

Placebo was taken orally 0.5g three times per day for 48 weeks, based on lifestyle intervention.

Lifestyle intervention is consisted of diet control and aerobic exercise. calorie restriction: to subtract 500 kcal from daily calorie intake aerobic exercise: medium intensity aerobic exercise for more than 150 min per week with heart rate around 50-70% of the maximal heart rate.

placebo tablets 0.5 tid, 30 minutes before each meal, for 48weeks

Hvad måler undersøgelsen?

Primære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Improvement in histologic features of nonalcoholic steatohepatitis by NAFLD activity score (NAS)
Tidsramme: 48 weeks

A separate system of scoring the histological features of nonalcoholic fatty liver disease (NAFLD) called the NAFLD Activity Score (NAS) was used. An improvement in histologic findings require an improvement by 1 or more points in the hepatocellular ballooning score; no increase in the fibrosis score; and either a decrease in the activity score for nonalcoholic fatty liver disease to a score of 3 or less or a decrease in the activity score of at least 2 points, with at least a 1-point decrease in either the lobular inflammation or steatosis score.

48 weeks

Sekundære resultatmål

Resultatmål
Foranstaltningsbeskrivelse
Tidsramme
Improvement in the composites of NAFLD activity scores for steatosis, lobular inflammation, hepatocellular ballooning
Tidsramme: 48 weeks

NAFLD activity score (NAS) is composed of steatosis (scale of 0 to 3), lobular inflammation (scale of 0 to 3), hepatocellular ballooning (scale of 0 to 2). Alteration in each component of NAS is measured.

48 weeks
Improvement in liver histological fibrosis staging
Tidsramme: 48 weeks

Fibrosis staging was measured as following criteria: 0=none, 1=perisinusoidal or periportal fibrosis, 2=perisinusoidal and portal/periportal fibrosis, 3=bridging fibrosis, and 4=cirrhosis.the definition of fibrosis stages improvement requires at least one stage.

48 weeks
Resolution of NASH
Tidsramme: 48 weeks

Resolution of NASH was defined as a diagnosis of no steatohepatitis at 48 weeks among those with possible or definite NASH at baseline.

48 weeks
Change in anthropometric measures
Tidsramme: 48 weeks

including BMI etc

48 weeks
Change in blood biochemistry
Tidsramme: 48 weeks

including serum aminotransferase levels etc

48 weeks
Change in liver fat content
Tidsramme: 48 weeks

liver fat content determined by 1H MRS (in part of clinical centers)

48 weeks
Change in serum cytokeratin 18 (CK-18) in U/L
Tidsramme: 48 weeks

serum cytokeratin 18 (CK-18) in U/L

48 weeks

Samarbejdspartnere og efterforskere

Det er her, du vil finde personer og organisationer, der er involveret i denne undersøgelse.

Sponsor

Samarbejdspartnere

Efterforskere

  • Ledende efterforsker: Xin Gao, Fudan University

Publikationer og nyttige links

Den person, der er ansvarlig for at indtaste oplysninger om undersøgelsen, leverer frivilligt disse publikationer. Disse kan handle om alt relateret til undersøgelsen.

Generelle publikationer

Datoer for undersøgelser

Disse datoer sporer fremskridtene for indsendelser af undersøgelsesrekord og resumeresultater til ClinicalTrials.gov. Studieregistreringer og rapporterede resultater gennemgås af National Library of Medicine (NLM) for at sikre, at de opfylder specifikke kvalitetskontrolstandarder, før de offentliggøres på den offentlige hjemmeside.

Studer store datoer

Studiestart (Faktiske)

16. august 2017

Primær færdiggørelse (Faktiske)

14. november 2024

Studieafslutning (Faktiske)

20. februar 2025

Datoer for studieregistrering

Først indsendt

18. juni 2017

Først indsendt, der opfyldte QC-kriterier

22. juni 2017

Først opslået (Faktiske)

26. juni 2017

Opdateringer af undersøgelsesjournaler

Sidste opdatering sendt (Faktiske)

23. september 2026

Sidste opdatering indsendt, der opfyldte kvalitetskontrolkriterier

19. september 2026

Sidst verificeret

1. marts 2025

Mere information

Begreber relateret til denne undersøgelse

Andre undersøgelses-id-numre

  • 2016ZSLC04

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