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Search / Trial NCT03749070

Efficacy of Silymarin in Patients With Non-alcoholic Fatty Liver Disease - The SILIVER Trial

Launched by CAMILA RIBEIRO DE AVELAR · Nov 19, 2018

Trial Information

Current as of May 08, 2025

Unknown status

Keywords

Non Alcoholic Fatty Liver Disease Sylimarin

ClinConnect Summary

Non-Alcoholic Fatty Liver Disease (NAFLD) is one of the most prevalent chronic liver diseases in Brazil. It has a significantly increasing incidence today and is considered an important global health problem. It affects approximately 20 to 30% of the adult population and increases according to the severity of the risk factors. The diagnosis of this disease usually occurs in 10 to 20% of the non-obese individuals, 50% in the overweight and 80 to 90% in the obese, being twice as present in individuals with Metabolic Syndrome. Pharmacological treatment options for NAFLD are still limited and S...

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Adults between 20 and 60 years of age, both men and women,
  • Clinical diagnosis of NAFLD, confirmed by imaging exams,
  • Exclusion Criteria:
  • Women in the menacing period, with the exception of those who have performed definitive sterilization, such as hysterectomy or tubal ligation.
  • Patients with established prior diagnosis of chronic noncommunicable disease (congestive heart failure, decompensated or severe lung disease, neoplasms, renal disease, advanced liver disease - Child Pugh C classification)
  • Patients with schistosomiasis;
  • Hemochromatosis
  • Wilson's disease
  • Viral or autoimmune hepatitis
  • HIV virus carriers
  • Woman who is breastfeeding
  • Users of illicit drugs
  • Patients with an intake of more than 20 g / day of alcohol and / or past alcoholism with abstention less than 6 months;
  • Patients with ingestion of medications such as steroids, estrogens, amiodarone, warfarin, anti-convulsants, antipsychotics, tamoxifen or other chemotherapeutic agents in the last 6 months
  • Patients with clinically manifest infections or inflammation, surgery, trauma or hospitalization in the last 30 days
  • Chronic non-hepatic degenerative diseases (sclerosis, Parkinson's disease or Alzheimer's disease)
  • Patients who do not participate in all stages of the research.

About Camila Ribeiro De Avelar

Camila Ribeiro de Avelar is a dedicated clinical trial sponsor with a strong commitment to advancing medical research and improving patient outcomes. With a background in clinical pharmacology and extensive experience in managing and overseeing clinical studies, she ensures that trials are conducted with the highest ethical standards and scientific integrity. Her focus is on fostering collaboration among multidisciplinary teams, facilitating innovative research methodologies, and adhering to regulatory compliance. Camila's leadership and expertise contribute to the successful development of therapies that address unmet medical needs, ultimately enhancing the quality of care in various therapeutic areas.

Locations

Salvador, Bahia, Brazil

Patients applied

0 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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