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临床试验/KCT0002259
KCT0002259招募中未知

Effects of herbal medicine for dysmenorrhea treatment on accompanied acne vulgaris: double-blind, randomized, parallel-group, multi-center trial

Kyung Hee University Oriental Medical Center0 个研究点目标入组 116 人开始时间: 待定最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
116

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 50(Year)(—)
性别
Female

入选标准

  • 1. Women aged over 19 years and in childbearing age
  • 2. Patients who have more than 10 inflammatory acne lesion on their face
  • 3. Patients who have menstrual pain more than grade 1 according to the verbal multidimensional scoring system
  • 4. Patients who have regular menstrual cycle from 23 days to 33 days within 3 months
  • 5. Patients who deteriorate acne vulgaris related to the menstrual cycle
  • 6. Patients who don’t have any problems for expressing their thoughts
  • 7. Written informed consent

排除标准

  • 1. Patients who taken following medicine
  • ? Topical or systemic corticosteroids (within 1 month)
  • ? Herbal medicine for acne treatment (within 1 month)
  • ? Nonsteroidal antiinflammatory drugs (NSAIDs) (within 2 weeks)
  • ? Oral contraceptives (within 1 month)
  • ? Topical or oral vitamin A derivatives (within 1 month)
  • ? Antibiotics (within 1 month)
  • ? Other unstable drugs as judged by the investigators
  • 2. Body Mass Index (BMI) <19 or BMI = 25
  • 3. Liver function abnormality (Aspartate aminotransferase (AST) or alanine aminotransferase (ALT)=60IU/L) or renal function abnormality (blood urea nitrogen (BUN)=30mg/dL or a serum creatinine levels = 1.5mg/dL)
  • 4. Pregnancy or breastfeeding or having plan to be pregnant or having possibility for pregnancy
  • 5. Patients who have malignant tumor, serious infection or severe systemic diseases
  • 6. Patients who attended to other clinical trials during previous 3 months
  • 7. unsuitability as judged by the investigators

研究者

发起方
Kyung Hee University Oriental Medical Center

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