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.
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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