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临床试验/CTRI/2024/08/071986
CTRI/2024/08/071986尚未招募3 期

Efficacy of a polyherbal formulation and life style modification in the management of yakritodar w.s.r to NAFLD - NI

Government of West Bengal0 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
3 期
状态
尚未招募

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

  • 1.Pain in the upper and epigastric region/pain in the right upper quadrant, fullness of abdomen, feeling of nausea and vomiting, loss of appetite, constipation etc.
  • 2.Elevated liver enzymes i.e. SGPT more than 1.5 times the normal value.
  • 3.USG evidence of hepatomegaly with fatty changes in liver.
  • 4. NAFLD Fibrosis score (NFS) range (less than -1.455 to 0.676).
  • 5.Diagnosed NAFLD and referred from other outpatient departments
  • 6. Patients who agreed to follow the study protocol and give constant for clinical trial.

排除标准

  • 1.Patient below 18 years and above 65 years.
  • 2.Patient who are not willing to come under trial or give consent.
  • 3.NAFLD Fibrosis score (NFS) range (more or equal to 0.676).
  • 4. Alcoholic steatohepatitis
  • 5. Alcoholic fatty liver (typically, a threshold of more than 20g/day for woman and more than 30g/day for men), ALT more or equal to 120 IU/L, total parental nutrition
  • 6. Liver cirrhosis/fibrosis, heart or renal failure.
  • 7. Underwent liver transplantation, gastrointestinal surgery.
  • 8.Vascular diseases of the liver, allergy, liver mass.
  • 9. H/o or presence of Type 1 DM
  • 10.Presence of any other form of chronic liver disease
  • 11.Hepatitis (A, B, C, D, E) positive patients
  • 12.Wilsons disease or metabolic liver disease
  • 13.Polycystic liver disease
  • 14.Cystic fibrosis of liver
  • 15.Non Alcoholic cirrhosis
  • 16.Auto immune hepatitis
  • 17.Primary and secondary Hepatic cellular Carcinoma (HCC)
  • 19.Gilbert disease
  • 20.alpha 1 antitrypsin deficiency
  • 21.Pregnant and lactating mother
  • 22.History of heart attack or stroke
  • 23.Mentally disabled patients

研究者

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