Clinical Trials Directory

Trials / Completed

CompletedNCT00820534

A Comparative Study of the Efficacy of Penciclovir 10mg/g (1%) Cream in Preventing the Appearance of Classical Lesion in Recurrent Cold Sore Sufferers

A Randomised, Double-blind, Vehicle Controlled, Single Center, Parallel Group, Comparative Study of the Efficacy of Penciclovir 10mg/g (1%) Cream in Preventing the Appearance of Classical Lesion in Recurrent Cold Sore Sufferers

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
126 (actual)
Sponsor
Novartis · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Comparison of the efficacy of penciclovir 10 mg/g (1%) cream with that of vehicle at 72 hours in preventing the appearance of classical lesions following prodromal symptoms (tingling or burning sensation) based on thermographic assessment among recurrent cold sore sufferers.

Conditions

Interventions

TypeNameDescription
DRUGPenciclovirPenciclovir every 2 hours during waking hours for 96 hours
DRUGPlaceboPlacebo every 2 hous during waking hours for 96 hours

Timeline

Start date
2008-12-01
Primary completion
2009-11-01
Completion
2009-11-01
First posted
2009-01-12
Last updated
2012-04-20
Results posted
2011-01-19

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00820534. Inclusion in this directory is not an endorsement.

A Comparative Study of the Efficacy of Penciclovir 10mg/g (1%) Cream in Preventing the Appearance of Classical Lesion in (NCT00820534) · Clinical Trials Directory