A study to determine the palatability of different dosage forms of oral N-Acetylcysteine and methionine among healthy volunteers
Not Applicable
- Conditions
- Palatability of antidotes to paracetamol poisoning
Recruitment & Eligibility
- Status
- Complete: follow up complete
- Sex
- Not specified
- Target Recruitment
- 30
Inclusion Criteria
1. Healthy male and female volunteers (who are not medical students)
2. Age 19-26 years
Exclusion Criteria
1. Condition or dietary habit known to interfere with the sense of smell and taste
2. Ingestion of any other medication within 48 hours
3. Significant illness within the previous two weeks
4. History of autonomic dysfunction
5. Atopic allergy
6. Known hypersensitivity to any drug
7. Pregnancy or breast feeding
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Each of the following outcomes will be scored on a modified 100 mm visual analogue scale. <br>1.1.Smell<br>1.2.Taste<br>1.3.Ease of swallowing <br>1.4. After taste<br>1.5. Adverse events within one hour [Just after the administration up to one hour]<br>
- Secondary Outcome Measures
Name Time Method one [None]<br>