CTRI/2023/05/052929尚未招募2 期
Efficacy of Ayurveda intervention in themanagement of menorrhagia (Raktapradara) â?? A Randomized control trial
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.Women age between 20-50 years.
- •2.Patient having regular (21-35 days) cycle with Heavy Menstrual Blood (HMB) loss, subjectively or objectively deï¬?ned (Pictorial Blood Assessment Chart â??PBAC3 score more than 100 points) or prolonged bleeding (bleeding more than >7days) for THREE consecutive cycles.
- •3.Patient willing to participate in study
排除标准
- •1.Hb % < 7gm%.
- •2.Lactating mother
- •3.Bleeding from the polyps, uterine fibroid, erosion and cancer.
- •4.Pregnancy and its Complication.
- •5.History of the bleeding from the site other than the uterus.
- •6.Women on Anti -Coagulant therapy.
- •7.Patient with raised liver enzymes twice the upper limit of normal & creatinine more than 1.4 mg%, poorly controlled Hypertension ( >160/100 mm of Hg), poorly controlled Diabetes Mellitus{B.S. (F) > 130 mg% and / or Blood Sugar (2 hr. PP) >250 mg% & HbA1c > 6.5%}.
- •8.Patients on Combined contraceptive pills/IUCD/DMPA
- •9.Patients on prolonged ( > 6 weeks) medication with corticosteroids, antidepressants, anti-cholinergics, anticoagulant etc. or any other drugs that may have an influence on the outcome of the study.
- •10.History of uncontrolled hyperthyroidism or hypothyroidism.
- •11.Patients who have a past history of Atrial Fibrillation, Acute Coronary Syndrome, Myocardial Infarction, Stroke or Severe Arrhythmia in the last 6 months.
- •12.History of tuberculosis, Pelvic Inflammatory Diseases (PID).
- •13.Patients with any other major systemic illness.
- •14.Patients who are currently participating in any other clinical trial
- •15.H/o hypersensitivity to the trial drug or any of its ingredients Any other condition which the Principal Investigator thinks may jeopardize the study.
- •16.Any other condition which the Principal Investigator thinks may jeopardize the study.
研究者
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