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临床试验/NCT03026569
NCT03026569已完成不适用

Orange Juice as Dietary Source of Antioxidants for Patients With Hepatitis C Under Antiviral Therapy

São Paulo State University2 个研究点 分布在 1 个国家目标入组 43 人开始时间: 2012年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
43
试验地点
2
主要终点
Total cholesterol

研究概览

简要总结

This study aimed to verify whether orange juice, source of citrus flavonoids and vitamin C, may contribute to the treatment of patients with chronic hepatitis C.

详细描述

Forty-three patients with chronic hepatitis C who were being treated with pegylated interferon combined with ribavirin, according to the Clinical Protocol and Therapeutic Guidelines for Viral Hepatitis C and Co-infections of the Brazilian Health Ministry were randomly divided into two parallel groups: (1) orange juice (n = 23), which were supplemented with orange juice (500 mL/d) for 8 weeks; (2) control group (n = 20) composed of patients that were not drinking orange juice regularly. The recruitment process began in February 2012, the intervention was carried out from May 2012 to July 2012, and the data analysis started in September 2012. The sample number took into account variances on total cholesterol with a type I error α = 0.05 and a type II error β = 0.2 (80% power) (Dourado et al., 2015). The minimum sample size should have 20 individuals per group (n = 40), considering an approximately 15% dropout rate. Primary and secondary endpoints were the reduction of total cholesterol and modification of biochemical markers, respectively. Kolmogorov Smirnov and Levene test assessed normality and homogeneity of data, respectively. Assessment of the data was performed in all participants on the first and last day of the experiment. All the parameters were compared between the juice group and the control group using General Linear Model of Repeated Measures Analysis. Differences in baseline patients' characteristics between the two groups were analyzed by One-way analysis of variance (ANOVA). The LSD signed rank post-test was used to assess significant changes in parameters after the start of treatment in each group, and the differences were considered statistically significant at p < 0.05.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Detection of circulating HCV RNA
  • Negative HBV surface antigen
  • Negative antibodies to HIV

排除标准

  • Co-infection with hepatitis B virus (HBV)
  • Co-infection with hepatitis A virus (HAV)
  • Co-infection with human immunodeficiency virus (HIV)
  • Presence of diabetes mellitus,
  • Presence of ascites
  • Elevation in serum ferritin levels

结局指标

主要结局

Total cholesterol

时间窗: 8 weeks

次要结局

  • Body mass(8 weeks)
  • Body mass index(8 weeks)
  • % body fat(8 weeks)
  • Waist circumference(8 weeks)
  • Glucose(8 weeks)
  • Insulin(8 weeks)
  • HOMA-IR(8 weeks)
  • LDL-C(8 weeks)
  • HDL-C(8 weeks)
  • Triglycerides(8 weeks)
  • CRP(8 weeks)
  • alkaline phosphatase(8 weeks)
  • AST(8 weeks)
  • ALT(8 weeks)
  • gamma-GT(8 weeks)
  • ABTS(8 weeks)
  • TBARS(8 weeks)

研究者

发起方
São Paulo State University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Thais Cesar

PhD

São Paulo State University

研究点 (2)

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