A Clinical Study to Evaluate the effect of Patha (Cissampelos pareira linn.) on Kashtartava W.S.R to Dysmenorrheoa

Himani1 个研究点分布在 1 个国家目标入组 30 人开始时间: 2021年9月15日最近更新: 2021年9月14日

试验速览

阶段: 不适用
状态: 尚未招募
发起方
入组人数: 30
试验地点: 1
主要终点: Menstruation is not painful anymore or is reduced to a substantial amount.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

this study is randomized open interventional study, to measure the efficacy of decoction of patha given at a dose of 50 ml twice a daily for three menstrual cycles that will be conducted in a single centre in india. The primary outcome measures will be the pacification or complete resolution of primary dysmenorrhea by decoction of patha. The secondary outcome will be no efficacy of decoction of patha in managing the pain of primary dysmenorrhea.

研究设计

研究类型: Interventional
分配方式: Adaptive randomization, such as minimization
盲法: Open Label

入排标准

年龄范围: 15.00 Year(s) 至 30.00 Year(s)（—）
性别: Female

入选标准

•Patients or parents of the young patients who agree to give written consent patients having chief complaint of painful menses patient suffering from primary dysmenorrhoea for more than 3 cycles.

排除标准

•Patients or parents of the young patients who do not agree to give written consent.
•Patient with chronic systemic illness and uterine pathology like fibroid, adenomyosis, endometriosis.
•Patient with intrauterine contraceptive devices.
•Patient suffering from hypothyroidism or Hyperthyroidism.

结局指标

主要结局

Menstruation is not painful anymore or is reduced to a substantial amount.

时间窗: 3 Months

次要结局

Menstruation is still painful to the same extent as before Intervention.(3 Months)

研究者

发起方

Himani

申办方类型

Other [Post Graduation scholar]

研究点 (1)

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