CTRI/2020/11/029406
Active, not recruiting
未知
A randomized, double blind, cross over, single center study to evaluate the oral sensory attributes of placebo tablet coatings
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- Abbott Healthcare Pvt Ltd
- Status
- Active, not recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. Healthy adult volunteer between 18 and 75 years of age at the time of enrolment who the Investigator believes that he/she can and will comply with the requirements of the protocol (e.g. study assessment completion).
- •2\.Female of childbearing potential must have a negative pregnancy test and be non\-lactating.
- •3\.Subject with no systemic or local conditions or on any medications that might compromise the taste or smell
- •4\.Subject who has never smoked, or who has smoked less than 100 cigarettes in his/her lifetime
- •5\.Subject signs and dates the written informed consent
- •6\.Agree to comply with the study procedures and requirements
Exclusion Criteria
- •1\.Female patients who are pregnant or a nursing mother
- •2\.Subject with any impairment in taste.
- •3\.Subjects who are determined as being the risk group for COVID\-19 as per applicable national guidelines.
- •4\.Subject who do not agree to comply with the study procedures
- •5\.Subject who is allergic to EazyGlideTM or conventional (Opadry) coatings or to the constituents of placebo tablets
Outcomes
Primary Outcomes
Not specified
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