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It is a Multicentric, Cross-sectional Survey to evaluate feedback based upon organolePtic propertiEs and compliance to marketed cough syRups prescribed in routine in clinical Practice.

Not Applicable
Conditions
Health Condition 1: J069- Acute upper respiratory infection,unspecified
Registration Number
CTRI/2022/06/043040
Lead Sponsor
Dr Reddys Laboratories Ltd
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Closed to Recruitment of Participants
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

Participants should meet below mentioned criteria to participate in the survey.

1.Subject 18 years and above

2.Willing and able to give data disclosure consent form.

3.Participant prescribed with cough syrup by treating physicians and willing to complete survey questionnaire

Exclusion Criteria

NONE

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
To evaluate and compare consumer survey response to the various cough syrups based on their organoleptic properties in routine clinical practice.Timepoint: There will be only 2 visits to site/clinic during participation in the survey. 2nd visit (Follow up visit) could be conducted onsite/ telephonic as applicable.
Secondary Outcome Measures
NameTimeMethod
oneTimepoint: None
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