Trials / Completed
CompletedNCT01265446
Efficacy and Safety of a Sore Throat Lozenge Containing Lidocaine and Cetylpyridinium Chloride in Patients With Sore Throat Due to a Common Cold.
A Randomized, Double-blind, Parallel Group, Single-dose Study of the Efficacy of Lidocaine 8 mg + Cetylpyridinium Chloride (CPC) 2 mg Fixed Combination Lozenges on Sore Throat Pain Intensity Compared to Lozenges Containing Lidocaine 1 mg and CPC 2 mg in Subjects With Sore Throat Due to Upper Respiratory Tract Infection.
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 250 (actual)
- Sponsor
- Novartis · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study will compare the efficacy and safety of a single dose of a lidocaine 8 mg + cetylpyridimium chloride (CPC) 2 mg lozenge with a single dose of a lidocaine 1 mg + CPC 2 mg lozenge in the treatment of sore throat due to a common cold.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Lidocaine 8mg + CPC 2mg | one single dose |
| DRUG | Lidocaine 1mg + CPC 2mg | one single dose |
Timeline
- Start date
- 2010-12-01
- Primary completion
- 2011-04-01
- Completion
- 2011-04-01
- First posted
- 2010-12-23
- Last updated
- 2013-04-24
- Results posted
- 2012-07-26
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT01265446. Inclusion in this directory is not an endorsement.