IRCT20231004059608N1招募中3 期
Assessment the Efficacy of Lactoferin as a Natural Product in Virus Clearance in HPV+ Patients: Randomized Double Blind Clinical trial
Pasture Institute of Iran0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 80
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
- 25 years 至 50 years（—）
- 性别
- Female
入选标准
- •Age: 25 to 50 years
- •Gender: Female
- •Marital Status: Married/Single
- •HPV positive patients (genotypes 16, 18, 31, 33, 39, 45, and 52)
- •Normal pap smear
- •Low grade pathology / CIN1
排除标准
- •Pregnant women
- •observation of internal/external warts
- •history of surgery
- •?alchohol consumption
- •AIDS (HIV+)
- •Drug use within 90 days
- •People with systemic immunosuppressive disorders
- •Patients who have received local or systemic treatment in the last three months.
- •Abnormal pap smear
- •High grade pathology
- •Conization history
- •Suffering from chronic diseases (diabetes, fatty liver and metabolic diseases, etc.)
- •Having more than 3 sexual partners
- •Patients with a history of treatment with Eldara and similar drugs (local and systemic)
- •History of Allergy, sensitivity to medicine, Anaphylaxis shock
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