CTRI/2023/02/049981已完成3 期
A clinical study to evaluate the effect of PanchasakaraChoorna in the management of Vibandha.
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 入组人数
- 30
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
- •Patient having symptoms of Vibandha (Constipation).
- •Patient who are fulfilling ROME IV Criteria for Constipation.
- •Patient who are fulfilling Bristol Stool Form Scale (1 to 2) for Constipation.
- •Only those patients willing to give the written informed consent.
排除标准
- •Patients on chronic laxative medication.
- •Patients on medicines which are intended to cause constipation (like Calcium supplements, Iron supplements, Diuretics, Opioids, Analgesics, Antidepressant).
- •Patients suffering with hypertension.
- •Pregnant or lactating women.
研究者
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