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临床试验/CTRI/2024/04/065391
CTRI/2024/04/065391已完成2 期

An Open Label, Randomized, Controlled Clinical Study to Evaluate the Therapeutic Efficacy of a Specific Unani Formulation in the Management of Non-Alcoholic Fatty Liver Disease (NAFLD)

Jamia Hamdard1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年4月26日最近更新:

试验速览

阶段
2 期
状态
已完成
发起方
Jamia Hamdard
入组人数
60
试验地点
1
主要终点
Improvement in Fatty liver grade assessed by QUS.

研究概览

简要总结

Patients of Non-Alcoholic Fatty liver Disease upto Grade II, fulfilling the Inclusion criteria and Exclusion criteria will be divided into two groups.

Group A patients will be given Unani formulation in a dose of 2 capsules twice daily orally in empty stomach for 90 days.

Group B patients will be given Vitamin E in a dose of 400 mg orally twice daily for 90 days.

The assessment of Primary objective (Fatty liver) will be done through QUS (Quantification Ultra Sound) on day 1 and day 90.

The assessment of LFT and Lipid profile will also be done on day 1 and day 90 to see the effect on secondary objectives.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients of grade 1 and grade 2 Fatty Liver (up-to 290 db/m in QUS/ Fibroscan)
  • Patients willing to participate and ready to sign the written informed consent.
  • Patients diagnosed as having fatty liver based on the ultrasonography report.
  • Patients with/ without clinical signs and symptoms.

排除标准

  • Patients having documented fatty liver grade 3 or above.
  • Use of alcohol or any other drug abuse.
  • Patients diagnosed with any coexisting liver disease.
  • Pregnant and lactating women.
  • Patients suffering with Hypertension, CKD, CAD, CLD or uncontrolled DM, Hypothyroidism.
  • Patient having immune-compromised status.
  • Patient using lipid lowering drugs or dietary supplements within the last 3 weeks.
  • Oral contraceptives & corticosteroids.
  • Neurological disorders like epilepsy or psychiatric disorders.
  • Acute hepatitis with raised serum bilirubin.

结局指标

主要结局

Improvement in Fatty liver grade assessed by QUS.

时间窗: 1st day and 90th day

次要结局

  • Improvement in Liver Function Test,(Improvement in Lipid profile)

研究者

发起方
Jamia Hamdard
申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Md Wasi Akhtar

Jamia Hamdard

研究点 (1)

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