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临床试验/CTRI/2021/02/031090
CTRI/2021/02/031090尚未招募2 期

A comparative clinical study of NÄ?gakesara CÅ«rnÌ£a and KutakÄ« CÅ«rnÌ£a in the management of AsrÌ£gdara with special reference to Dysfunctional Uterine Bleeding.

ational Institute of Ayurveda0 个研究点目标入组 0 人开始时间: 待定最近更新:

试验速览

阶段
2 期
状态
尚未招募

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

  • 1) Patients ready to participate in the clinical trial.
  • 2) Patients diagnosed as dysfunctional uterine bleeding.
  • 3) Excessive menstrual bleeding (amount >80 ml) or Prolonged menstrual bleeding ( >7 days) with or without heavy flow or Frequent menstrual cycle (interval < 21 days)
  • 4) Patients presenting with inter-menstrual bleeding with or without heavy flow for 2 consecutive cycles.

排除标准

  • 1) Patients with chronic systemic illness (Congestive cardiac failure, Hypertension, cirrhosis of liver, Tuberculosis endometritis, severe anaemia, chronic renal disease, Insulin dependent diabetes mellitus etc.).
  • 2) Patients using Intrauterine contraceptive device or oral contraceptive pills (Iatrogenic).
  • 3) Patients with uterine and pelvic pathology (Fibroid size >2 cm, endometriosis, adenomyosis, polyp, high grade cervical erosion, endometrial thickness >20 mm etc.).
  • 4) Congenital malformations of uterus(Septate uterus, double uterus).
  • 5) Benign and malignant growth.
  • 6) Thyroid dysfunction (endocrinal disorders).
  • 7) Patients having bleeding due to abortion, ectopic pregnancy, during puerperium.
  • 8) Patients taking Anti-coagulation therapy and having haematological disorders (Leukemia, Thrombocytopenic Purpura).
  • 9) Postmenopausal bleeding.
  • 10) Sexually transmitted infections/Genital tract infections.

研究者

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