跳至主要内容
临床试验/CTRI/2019/06/019592
CTRI/2019/06/019592已完成4 期

Comparative Effectiveness of Ranolazine and Saroglitazar on Non-Alcoholic Fatty Liver Disease in Patients with Diabetic Dyslipidemia: A Randomized controlled open label trial

Self0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
Self

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

入选标准

  • Had ALT above upper limits of normal (19 U per
  • L for women, 30 U per L for men).
  • -Had ALD or NAFLD Index less than 0.
  • -Had documented hepatic steatosis (Fatty Liver
  • Index greater than equal to 60, NAFLD-FAT
  • SCORE greater than minus 0.640, Hepatic
  • steatosis index greater than equal to 36,
  • NAFLD fibrosis score less than minus
  • 1.455,Liver Accumulation Product greater than
  • equal to 80).
  • -HbA1C greater than equal to 7%
  • -Willingness to comply with all protocol
  • required evaluations; provision of written
  • informed consent before any study specific
  • tests or procedures are performed.

排除标准

  • -Presence of other chronic liver diseases
  • (hepatitis B or C, autoimmune hepatitis,
  • cholestatic liver disease, Wilsons disease,
  • hemochromatosis, etc.).
  • -Average alcohol consumption greater than equal
  • to 21 drinks per week formen, greater than
  • equal to 14 drinks per week for women in the 6
  • months before enrollment.
  • -The patients who already used medications
  • known to cause hepatic steatosis for more than
  • two weeks in the past year such as mipomersen,
  • lomitapide, amiodarone, methotrexate,
  • tamoxifen, corticosteroid, valproate,
  • antiretroviral medicines.
  • -Presence of alternative cause of fatty liver,
  • including Total Parenteral Nutrition,
  • Starvation, Lipodystrophy,
  • -Abetalipoproteinemia, Acute fatty liver of
  • pregnancy, HELLP syndrome, Reyeââ?¬•s syndrome.
  • Clinical, imaging, or histological evidence of
  • -Use of drugs with a potential effect on NASH
  • such as ursodeoxycholic acid, vitamin E,
  • pioglitazone.
  • -Pregnant or lactating female.

研究者

发起方
Self

相似试验