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临床试验/IRCT201705309472N13
IRCT201705309472N13招募中2 期

Effect of saffron powder on serum concentration of hs-CRP, TNF-a, MDA, TAC, adiponectin and leptin in patients with non-alcoholic fatty live disease

Deputy of Research of Iran University of Medical Sciences0 个研究点目标入组 76 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
76

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

年龄范围
18 years 至 65 years(—)
性别
All

入选标准

  • Inclusion criteria
  • 1- Age 18 to 65 years
  • 2. Both sexes
  • 3. Detection of non-alcoholic fatty liver by an expert physician based on the high levels of ALT, AST enzymes
  • >=30U / L in men and> 19U/L in women) and liver transcription
  • 4. Desire to participate in studying and signing conscientious intention
  • Non-inclusion criteria: (exclusion criteria)
  • 1- Pregnancy and lactation or planning pregnancy
  • 2- Use an antioxidant supplement or any nutritional supplement within one month before sampling
  • 3. Acute heart disease, kidney, thyroid, diabetes, infections, hepatitis B and C and other liver diseases (diagnosed by a specialist) and diseases that affect the weight (hyperprolactinemia, Cushing's syndrome)
  • 4. Have a high-gain or weight loss regimen within 3 months prior to sampling
  • 5- Using effective drugs on weight, fatty liver and insulin resistance during 3 months before sampling (hormonal, antidepressant, anti-psychotics)
  • 6- Use of drugs that are probably related to NAFLD:
  • 7- (valporic acid, tetracycline, systematic glucocorticoid, methotrexate amidarone, anabolic steroids, estrogen, tamoxifen or other known hepatotoxic drugs)
  • Exit criteria:
  • 1. Unwillingness to continue cooperation in research
  • 2- Initiating the use of anti-NASH drugs (thiazolidindiones, vitamin E, betaine, milk thistle, UDCA, SAM-E, gemfibrozil, probiotic, anti-TNF-a)
  • 3. Start using any type of nutritional supplement and anti-inflammatory drugs
  • 4. Cure for diseases that require special treatments that interfere with the intervention.
  • 5- Pregnancy during the study
  • 6- Patients whose compliance and consumption of saffron powder or placebo by them is less than 80% recommended by the host.

排除标准

  • 未提供

研究者

发起方
Deputy of Research of Iran University of Medical Sciences

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