CTRI/2025/08/092381尚未招募3 期
To evaluate the efficacy of Chaturbeeja churna and Dashamularista in sutika paricharya a comparative study
Minuwara Khatun1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2025年9月1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
- 60
- 试验地点
- 1
- 主要终点
- Decrease in symptoms like
研究概览
简要总结
This is a comparative study to evaluate the clinical efficacy of Chaturbeeja churna with Dashamularishta in Sutika paricharya. Total 60 patients to be studied in 3 groups. In each group 20 patients will be selected. First group will be given Dashamularishta, second Chatubeeja churna and third group will be given both Chatubeeja churna and Dashamularishta for 45 days each. Patients will be followed up on 15th day till completion of treatment.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 20.00 Year(s) 至 45.00 Year(s)（—）
- 性别
- Female
入选标准
- •1.Sutika of age 20 to 45 years.
- •2.Spontaneous vaginal delivery.
排除标准
- •1.Puerperial woman with history of LSCS.
- •2.Postpartum hemorrhage.
- •3.Systemic and infectious disorders.
- •4.Hb% below 8 grams.
结局指标
主要结局
Decrease in symptoms like
时间窗: 15 days
1.Purisha avarodh(constipation)
时间窗: 15 days
2.Nidrahani(insomnia)
时间窗: 15 days
3.katishool(backache)
时间窗: 15 days
4.parshwashool(pain in flanks)
时间窗: 15 days
5.angamarda(bodyache)
时间窗: 15 days
次要结局
- Complete cessation of purisha avarodh and other associated symptoms like-(1.katishool(backache))
研究者
Minuwara Khatun
Govt Ayurvedic College and Hospital, Gauhati
研究点 (1)
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