CTRI/2020/06/025559Completed未知
A single centre, prospective, randomized, open labelled clinical study to evaluate the effectiveness of Siddha herbal formulation, Vipro, in uncomplicated respiratory infections
Trial Snapshot
- Phase
- 未知
- Status
- Completed
- Sponsor
- Buy Happy Marketing LLP
- Enrollment
- 60
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1. Having uncomplicated respiratory infections, at least for less than 5 days, diagnosed with clinical symptoms and signs of fever, myalgia, rhinitis, sore throat, throat pain, cough, expectoration and head ache
- •2. Consenting to participate in the study and sign the informed consent
Exclusion Criteria
- •1. Patients with uncontrolled co-morbid conditions like Diabetes mellitus, Hypertension and Bronchial asthma
- •2. Patients with Lower respiratory tract infections, Chronic Bronchitis, Chronic obstructive air way problems
- •3. Patients with significant Cardiovascular, Neurological , Psychiatric, Gastro intestinal and other system infections or disorders and malignancies
- •4. Hypersensitivity to the herbal ingredients in the formulations and other medications prescribed in the study
- •5. Pregnant and feeding mothers
- •6. When the patients are interviewed for selection, all those patients who come under the testing criteria for COVID-19 as per ICMR guidelines will be tested for COVID â?? 19 and if they are found to be positive, they will be excluded from participating in the study.
Investigators
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