CTRI/2022/12/048144已完成未知
An Open label clinical study to evaluate the safety and efficacy of molecular medicine and CelWel
Carmel Research Consultancy Private Limited0 个研究点目标入组 15 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 15
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
- •1.Patients with long covid symptoms
- •2.Male and female subjects ranging in age from 18
- •to 99 years.
- •3.Willingness to follow the protocol requirements
- •as evidenced by written, Informed Consent.
- •4.Mentally, physically and legally eligible to
- •give informed consent.
- •5.Willingness to complete study questionnaires.
排除标准
- •1.Patients with pre-existing other severe systemic
- •disease necessitating long-term medication.
- •2.History of cancer, including solid tumours,
- •hematologic malignancies and carcinoma in situ
- •3.Any vascular or systemic disorder which could
- •affect any of the efficacy assessments
- •4.Subjects received other medication (anti-viral)
- •within the 36 hours before entry into the study
- •5.Evidence of significant uncontrolled co-morbid
- •disease which would jeopardize patient
- •participation
- •6.Patients hospitalized or requiring oxygen
- •7.Patients unable to take oral medication
研究者
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