IRCT20120215009014N376尚未招募3 期
Effect of N-acetyl cysteine supplementation versus placebo on clinical outcomes in women with chronic pelvic pain syndrome: a double-blind randomized clinical trial
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 60
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 50 years（—）
- 性别
- Female
入选标准
- •Age of 18 to 50 years,
- •Women with chronic pelvic pain syndrome for at least 6 months,
排除标准
- •Presence of pathologic or infamous reason for chronic pelvic pain,
- •Mild symptoms (the score less than 15 based on NIH-CPSI questionnaire),
- •Chronic liver or renal disease,
- •Kidney stone or urogenital tract infection,
- •History of surgery of urogenital tract,
- •Contraindication of N-acetyl cysteine
研究者
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