CTRI/2023/07/054617尚未招募3 期
Effectiveness of Rajapravartani Vati and Saraswatarishta in Dysmenorhoea - A prospective community based study - Nil
试验速览
- 阶段
- 3 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
- •i.Women of age 14 -25 years with self-reported history of menstrual pain of moderate to severe nature (as per WaLIDD score) (Annexure I)
- •ii.At least 3 painful cycles in last 6 cycles
- •iii.Having normal menstrual cycle (21-35 days) with normal menstrual bleeding (3-7 days) during last 3 cycles
- •iv.Participants willing to provide written informed consent/ assent for their participation in the study for 6 months.
排除标准
- •i.Irregular Cycles.
- •ii.Cases of secondary Dysmenorrhea [Known case or h/o of leiomyoma of uterus, ovarian cyst, endometriosis. pelvic inflammatory disease (PID)]
- •iii.Pain abdomen associated with excessive bleeding per vagina.
- •iv.Presence of persistent pelvic pain throughout the menstrual cycle.
- •v.Associated with any pre-diagnosed or clinically diagnosed systemic disorders likely to influence menstrual cycle.
- •vi.Participants with Hb <10 gm %
- •vii.History of malignancy of pelvic organs.
- •viii.Diagnosed cases Hypothyroidism /hyperthyroidism
- •ix.Woman using IUD / Oral Contraceptive Pills (OCP)
- •x.Participants having blood pressure = 160/100 mmHg, &/or HbA1C >8 %
- •xi.Participants with concurrent serious hepatic disorder (defined as Aspartate AminoTransferase (AST) and / or Alanine Amino Transferase (ALT), Total Bilirubin, Alkaline Phosphatase (ALP) > 2 times upper normal limit) or Renal Disorders (defined as S. Creatinine > upper normal limit)
- •xii.Participants with diagnosed concurrent neurological, pulmonary or endocrine disorder, or unstable cardio-vascular disease
- •xiii.Women who are planning to conceive in the next 6 months
- •xiv.Lactating women
- •xv.Participation in other concomitant therapy for acute or chronic pain.
研究者
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