CTRI/2023/08/056384尚未招募不适用
Clinical Study To Evaluate The Efficacy Of Bhagottar Gutika And Abhyanga In The Management Of Post COVID Respiratory Distress
Ajit kumar pandey1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2023年11月8日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- It is expected that at the end of study we would be able to demonstrate the efficacy of BhagottarGutika & Abhyanga with
研究概览
简要总结
BhagottarGutika a herbomineral preparation and Abhyanga with
Amrutadi tailam will be done the management of Post covid respiratory distress .
研究设计
- 研究类型
- Interventional
- 分配方式
- Random Number Table
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 58.00 Year(s)（—）
- 性别
- All
入选标准
- •1 Age between 18 to 58 years irrespective of sex.
- •2 Previously confirmed cases of SARS Cov-2 Rt-PCR patients.
- •3 Post covid Patients presented with symptoms such as SOB, fatigue and insomnia.
- •At least two symptoms must be present out of which one must be SOB.
- •4 FEV1 greater than 80% of the predicted value.
- •5 Patients willing to give written consent for participation in the study.
排除标准
- •1 Patients having major systemic illness, renal, hepatic and Autoimmune diseases.
- •2 Patients who are immunocompromised such as chronic DM and HIV etc.
- •3 Pregnant and lactating mothers.
结局指标
主要结局
It is expected that at the end of study we would be able to demonstrate the efficacy of BhagottarGutika & Abhyanga with
时间窗: 30 days
Amrutaditailam in the management of PCRD.
时间窗: 30 days
次要结局
- this study will helpful in treating respiratory distress patient(15th 30th & 45th day of study)
研究者
研究点 (1)
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