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Completed

NCT Number: NCT04038853

Vitamin D in Fatty Liver Disease

This study evaluates the influence of vitamin D in reducing laboratory, elastographic (Fibroscan) and metabolic components of NAFLD. Half of the patients will receive vitamin D (Plivit D3) while the other half will receive placebo

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Key information

About this study

In this study will participate patients who come to the regular ambulatory examinations (referred by gastroenterologists, or family physicians in the Department of Gastroenterology CHC Rijeka) and have one or more components of the metabolic syndrome (hypertension, diabetes, obesity, dyslipidemia).Nonalcoholic fatty liver disease will be defined by transient elastography (FibroScan, Echosens, Paris); Controlled Attenuation Parameter (CAP) for assesment of liver steatosis and Liver Stiffness Measurements (LSM) for liver fibrosis. In all patients other causes of chronic liver disease will be excluded; chronic viral hepatitis, autoimmune diseases and other metabolic liver diseases as well as use of drugs than can cause liver steatosis and fibrosis and alcoholic liver disease.

This study will include 450 patients. Taking into account the possible drop-out rate around 15% of the patients during the study period, a total of 400 patients will be randomized. Patients will be randomized into two groups. The first group will be consisted of the patients with NAFLD who will be receiving original medication during the 12 month period. The second group will be consisted of the patients with NAFLD who will be receiving placebo during the 12 months period, which will be identical to the original medication in its packaging and form.

After the 6 and 12 months of therapy in all patients will be evaluated: liver enzymes and metabolic laboratory parameters of NAFLD (insulin resistance, lipidogram and serum glucose), as well as the TE-CAP in order to evaluate the efficiency of Plivit D3 for the treatment of NAFLD.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • patients with Non-Alcoholic Fatty Liver Disease (NAFLD)
  • signed informed consent
  • possibility to follow instruction and the protocol

Exclusion criteria

  • chronic B or C hepatitis
  • usage of hepatotoxic drugs in the period of 6 months before inclusion
  • chronic kidney insufficiency (grade 4 and 5), hemodialysis
  • any other chronic liver disease
  • opioid dependancy
  • any malignancy
  • HIV seropositivity
  • alcohol abuse
  • pregnancy
  • inability to follow the protocol

Treatment and study plan

1,25-Dihydroxyvitamin D

Drug

1,25-dihydroxy-vitamin D3 1000 IU orally daily for 12 months

Other names: 1,25-Dihydroxy-Cholecalciferol, Cholecalciferol, Vitamin D3

Placebo

Drug

Placebo identical to the study intervention drug

Primary outcomes

  1. Elastographic parameter of steatosis

    Time frame: Week 0 - initiation; after 6 months; and after 12 months (end of study)

    Change of elastographic parameter of steatosis (Controlled Attenuation Parameter; CAP) during the 6 and 12 months period

  2. Elastographic parameter of fibrosis

    Time frame: Week 0 - initiation; after 6 months; and after 12 months (end of study)

    Change of elastographic parameter of fibrosis (liver stiffness measurements; LSM) during the 6 and 12 months period

Secondary outcomes

  1. Aspartate transaminase

    Time frame: Week 0 - initiation; after 6 months; and after 12 months (end of study)

    Change in liver enzyme aspartate transaminase (AST) serum levels in the period of 6 and 12 months. Normal range = 11-38 IU/L.

  2. Alanine transaminase

    Time frame: Week 0 - initiation; after 6 months; and after 12 months (end of study)

    Change in liver enzyme alanine transaminase (ALT) serum levels in the period of 6 and 12 months. Normal range = 12-48 IU/L.

  3. Gamma-glutamyl transferase

    Time frame: Week 0 - initiation; after 6 months; and after 12 months (end of study)

    Change in liver enzyme gamma-glutamyl transferase (GGT) serum levels in the period of 6 and 12 months. Normal range = 11-55 IU/L.

  4. Insuline Resistance

    Time frame: Week 0 - initiation; after 6 months; and after 12 months (end of study)

    Change in insulin resistance defined by the Homeostatic Model Assessment for Insulin Resistance (HOMA-IR; normal range = 0.5 to 1.4) score in the period of 6 and 12 months

  5. Total cholesterol

    Time frame: Week 0 - initiation; after 6 months; and after 12 months (end of study)

    Change in total cholesterol serum levels in the period of 6 and 12 months

  6. Low-density lipoprotein

    Time frame: Week 0 - initiation; after 6 months; and after 12 months (end of study)

    Change in low-density lipoprotein (LDL) serum levels in the period of 6 and 12 months

  7. High-density lipoprotein

    Time frame: Week 0 - initiation; after 6 months; and after 12 months (end of study)

    Change in high-density lipoprotein (HDL) serum levels in the period of 6 and 12 months

  8. Triglyceride

    Time frame: Week 0 - initiation; after 6 months; and after 12 months (end of study)

    Change in triglyceride (TG) serum levels in the period of 6 and 12 months

Sponsors and collaborators

Lead sponsor

University Hospital Rijeka

Other

Collaborators

  • Pliva Hrvatska d.o.o.
  • University of Rijeka

Registry information

Official study title

Use of Vitamin D in Treatment of Non-Alcoholic Fatty Liver Disease Detected by Transient Elastography

Important dates

Study start
2015
Primary completion
2017
Study completion
2019
First posted
Jul 31, 2019
Registry last updated
Jul 31, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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