Strepsils Flavour Variant Efficacy Study
Research type
Research Study
Full title
A multi centre, randomised, double blind, placebo-controlled, parallel group, single dose study of the efficacy of two flavour variants of Strepsils throat lozenges in the relief of sore throat due to upper respiratory tract infection.
IRAS ID
8455
Sponsor organisation
Reckitt Benckiser Healthcare, UK Ltd
Eudract number
2008-00-5596-10
Research summary
This study will examine the effects of two new flavour variants of Strepsils lozenges versus anon-medicated placebo in subjects with a sore throat over a period of 2 hours. Subjects with a sore throat who are eligible to take part in the study will receive a lozenge in the clinic. Subjects will complete self-assessment forms which consist of throat soreness scores, difficulty in swallowing scales, throat numbness and a sore throat pain relief scale at regular intervals over a period of 2 hours. Additional questions regarding consumer acceptability of the product will also be contained in a consumer questionnaire. Once the 2 hour study assessment period is complete subjects can seek to treat their sore throat as required.
REC name
East of Scotland Research Ethics Service REC 2
REC reference
08/S0501/91
Date of REC Opinion
18 Nov 2008
REC opinion
Favourable Opinion