Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT00670696

A Study to Compare the Efficacy of Rapydan Versus Tetracaine Gel

A Randomised, Controlled, Single-blinded, Cross Over Comparison Study to Compare the Efficacy of the Rapydan Medicated Plaster Versus Tetracaine Gel

Status
Withdrawn
Phase
Phase 4
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Jazz Pharmaceuticals · Industry
Sex
Male
Age
18 Years
Healthy volunteers
Accepted

Summary

Tetracaine gel 4% is a topical anaesthetic gel commonly used in the UK that contains 40 mg of tetracaine base per gram. Adequate anaesthesia can usually be achieved following a 30 minute application time for venopuncture and a 45 minute application time for venous cannulation. The hypothesis is that Rapydan medicated plaster is more effective than tetracaine gel in preventing venous cannulation related pain when applied for the recommended treatment durations of 30 minutes and 45 minutes respectively.

Detailed description

Tetracaine gel 4% is a topical anaesthetic gel commonly used in the UK that contains 40 mg of tetracaine base per gram. Adequate anaesthesia can usually be achieved following a 30 minute application time for venopuncture and a 45 minute application time for venous cannulation. The hypothesis is that Rapydan medicated plaster is more effective than tetracaine gel in preventing venous cannulation related pain when applied for the recommended treatment durations of 30 minutes and 45 minutes respectively. This study has been withdrawn and no additional data is available.

Conditions

Interventions

TypeNameDescription
DRUGRapydanTopical anaesthetic plaster
DRUGtetracaine gelTopical tetracaine gel

Timeline

Start date
2008-04-01
Primary completion
2008-12-01
First posted
2008-05-02
Last updated
2012-04-25

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT00670696. Inclusion in this directory is not an endorsement.