CTRI/2022/01/039180
Completed
Phase 2
A randomized, controlled clinical study to compare efficacy of a polyherbal formulation (GP/PROD/2021/004) versus Standard Allopathic Formulation for relief of acutenonproductive cough and throat irritation - Nil
Mr Kamlesh Thummar0 sites66 target enrollmentStarted: TBDLast updated:
Overview
- Phase
- Phase 2
- Status
- Completed
- Sponsor
- Mr Kamlesh Thummar
- Enrollment
- 66
Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •Patients with H/O acute nonproductive cough and throat irritation for less than 1week duration
- •Males and Females between 18\-65 years age
- •Patients who in the opinion of the Investigator will be able to comply with the study requirements
- •Patients with a cough score of 0, 1 or 2 during day time
- •Patients willing and able to provide signed informed consent for any study related procedures.
Exclusion Criteria
- •Patients with H/O lower respiratory tract infections such as Pneumonia, Tuberculosis, Bronchitis, Whooping cough.
- •Patients with H/O Chronic Obstructive Pulmonary
- •Diseases/Asthma
- •Patients with H/O underlying lung pathology such as lung abscess, cystic fibrosis.
- •Patients with known hypersensitivity to ingredients of Investigational Products
- •Patients with clinical suspicion of any systemic bacterial infection.
- •Patients with H/O Myocardial Infarction (MI) within 4 weeks prior to enrollment
- •Patients with immediate life threatening diseases such as pre\-existing cardiovascular, liver or neoplastic disease.
Investigators
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