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A Trial to Assess the Safety and Efficacy of Topical Salbutamol in Healthy Volunteers. — SSCART  

Scarring Clinical Trial

Official title:
A Double Blind, Placebo Controlled, Randomised Dose Escalation Trial to Investigate the Safety and Efficacy of Topical Salbutamol in the Improvement of Scar Appearance When Applied to Approximated Wound Margins in Healthy Volunteers.

Clinical Trial Summary

This will be a single centre, double-blind, placebo (vehicle) controlled, randomised, dose escalation trial. Three concentrations of topical salbutamol gel will be compared, in a group-wise fashion, with a placebo administration at one incision site on each arm of the trial subjects. Each participant will be allocated to only one dosing group. The treatments will be paired anatomically so that for each pair of sites, one closed incision site will receive the active substance, while the other will receive placebo.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03514615
Study type Interventional
Source University Hospitals, Leicester
Contact
Status Completed
Phase Phase 1
Start date January 10, 2018
Completion date July 1, 2019
View Details
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