A study to determine the palatability of different dosage forms of oral N-Acetylcysteine and methionine among healthy volunteers

Not Applicable

Completed

• Conditions: Palatability of antidotes to paracetamol poisoning

• Registration Number: SLCTR/2016/001
• Lead Sponsor: South Asian Clinical Toxicology Research Collaboration

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 2024-08-20

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