CTRI/2021/03/031815尚未招募3 期
A clinical study to evaluate the effect of livance-c, an anti-viral ayurvedic formulation for the treatment of covid-19 patients
Avance Phytotherapies Pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
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
- •Freshly detected and confirmed positive (by means of RT-PCR) COVID-19 patients requiring admission.
- •Patients on whom no other (specifically targeted to treat COVID-19) treatment has been initiated. (Patients on supportive care can be considered for inclusion).
- •Patients who have consented (written informed consent) to be treated
- •with the trial drug as the primary treatment.
- •Patient is in the age group between 18-65years.
- •Patient has persistent fever >=99.50 F and is currently maintained on
- •antipyretics.
- •Patient is unable to take a deep breath and/ or not able to hold for >= 20
- •Patient has a history of cough since >= 3 days.
- •Patient has a history of body aches or tiredness or unusual fatigue lately
- •(>= 7 days).
- •Patients ability in the investigators opinion to comply with the protocol
- •procedures.
排除标准
- •Suspected patients with COVID19, but not confirmed by RT-PCR test.
- •Confirmed positive Patient on whom already alternative medical treatment has been initiated.
- •History of tuberculosis.
- •History / evidence of allergy or hypersensitivity to Hydroxychloroquine sulfate or of herbal drugs or to any of the inactive ingredients of the formulation or to any other drug.
研究者
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