CTRI/2023/06/053524尚未招募3 期
Evaluation of the efficacy of shatapushpa taila nasya in the management of artava kshaya
DR ANUDEEPA NATH1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2023年6月25日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Decrease In Symptoms Of Artava Kshaya Like
研究概览
简要总结
THIS IS AN EFFECTIVENESS OF SHATAPUSHPA TAILA IN THE FORM OF NASYA IN THE MANAGEMENT OF ARTAVA KSHAYA . THIS IS DONE COMPULSORY PART OF POST GRADUATE COURSE. TOTAL NUMBER OF PATIENTS TO BE STUDIED IS 30 WITH DURATION OF 30 DAYS.
研究设计
- 研究类型
- Interventional
- 分配方式
- Adaptive randomization, such as minimization
- 盲法
- Open Label
入排标准
- 年龄范围
- 18.00 Year(s) 至 45.00 Year(s)（—）
- 性别
- Female
入选标准
- •Infrequent Menses At Interval Between Two Cycle Exceeding More Than 35 Days
- •Reduced Quantity Of Flow That Is Using Less Than 2 Pads Per Day 3.Artava Kshaya Due To PCOD 4.Duration Of Flow Less Than Two Days 5.Irrespective Of Marriage.
排除标准
- •Pregnant Women Lactating Women Patient Having Systemic Disorders Hyperthyroidism Severe Anaemia hb level Less Than 7Gm/Dl Any Type Of Malignancy.
结局指标
主要结局
Decrease In Symptoms Of Artava Kshaya Like
时间窗: 3 months
To Normalise The Duration Of Bleeding
时间窗: 3 months
Normalise The Interval Between Two Cycles
时间窗: 3 months
MInimise The Grade Of Pain
时间窗: 3 months
To Normalise The Amount Of Blood Loss
时间窗: 3 months
次要结局
- Ultrasonography of lower abdomen to be within normal limit(TSH T3 T4)
研究者
研究点 (1)
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