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临床试验/CTRI/2019/01/017118
CTRI/2019/01/017118已完成未知

Effect of Bisfayej in Premenstrual Syndrome: A Randomised Controlled Study -

ational Institute of Unani Medicine0 个研究点目标入组 66 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
已完成
发起方
入组人数
66

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

入选标准

  • Patients having a regular spontaneous menstrual cycle of 21 to 35 days presenting with signs and symptoms of premenstrual syndrome.
  • Patients having symptoms of PMS for atleast 3 menstrual cycles as per ACOG guidelines.

排除标准

  • Patients presenting with irregular menstrual cycle.
  • Patients on oral contraceptives and lactating women.
  • Patients having any unstable medical illness and seizure disorder.
  • Diagnosed cases of psychosocial stresses, family, mood andpersonality stresses or depression disorders.
  • Patients with any systemic and endocrineillness like diabetes mellitus, thyroid dysfunction.

研究者

发起方
ational Institute of Unani Medicine

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