To evaluate and compare different properties of cough syrup and its compliance after one use.
Not Applicable
- Registration Number
- CTRI/2021/04/032872
- Lead Sponsor
- Dr Reddys Laboratories Ltd
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Other (Terminated)
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Healthy Men and Women
Ready to abide with the protocol and willing to sign the informed consent document
Exclusion Criteria
Pregnancy by / Lactating Women.
Having health issues and on medication.
Addiction issues, alcohol abusers, smokers.
Having allergies to any constituent of the cough syrups
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Identification of difference in Organoleptic properties by DISCRIMINATION/ DIFFERENCE TEST. <br/ ><br> <br/ ><br>Measurement of Intensities in Organoleptic properties by SCALING TEST (4 point). <br/ ><br> <br/ ><br>Evaluation of Acceptability through Paired Comparison on 9-point Scale (JUST RIGHT HEDONIC TEST). <br/ ><br> <br/ ><br>Evaluation of Subject Compliance based on the Organoleptic properties and overall acceptability of the products. <br/ ><br>Timepoint: After consumption of each product
- Secondary Outcome Measures
Name Time Method ILTimepoint: NI