CTRI/2021/02/031090
Not yet recruiting
Phase 2
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.
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- ational Institute of Ayurveda
- Status
- Not yet recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •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.
Exclusion Criteria
- •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.
Outcomes
Primary Outcomes
Not specified
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