PACTR201609001765772已完成未知
The Clinical Outcome of the Combination Regimen of Ginkgo biloba Extract with Ursodeoxycholic acid in Chronic Hepatitis C Egyptian Patients
Dina Mohamed kamal El-Gindy0 个研究点目标入组 67 人开始时间: 2016年9月5日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 67
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 Year(s) 至 65 Year(s)（—）
- 性别
- All
入选标准
- •positive serum anti-HCV Ab and HCV RNA
- •clinical and ultrasonographic criteria suggestive of chronic hepatitis C
- •Elevation of ALT at least 1.5 times the upper limit of normal (but < 5 times the normal limit)
- •Child Pugh Grade A
排除标准
- •Child Pugh Grade was B or C
- •had other causes of liver disease or had evidence of advanced liver disease e.g. history or presence of ascitis, bleeding esophageal varices, or hepatic encephalopathy.
- •had portal vein thrombosis, hepatocellular carcinoma, seizure disorders
- •body mass index >40
- •advanced systemic disease like heart failure or any debilitating disease that will affect life expectancy
- •using oral contraceptive pills, selective serotonin reuptake inhibitors, narcotic drugs, blood thinning drugs or those who received a treatment of antiviral agents (interferon with or without ribavirin) in the previous 2 months.
- •pregnancy or lactation
- •patients with platelet level <50,000/µL patients with sensitivity to UDCA or EGb.
研究者
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