Clinical Trials Directory

Trials / Terminated

TerminatedNCT00162786

Comparative Effects of Rupatadine 10 mg, Hydroxyzine 50 mg and Placebo on Actual Driving Performance

Status
Terminated
Phase
Phase 4
Study type
Interventional
Enrollment
20 (planned)
Sponsor
J. Uriach and Company · Industry
Sex
All
Age
21 Years – 35 Years
Healthy volunteers
Accepted

Summary

The primary objective of this study is to measure and compare the acute effects of rupatadine 10 mg, relative to placebo and hydroxyzine 50 mg as an active control on healthy volunteers' performance on a standard over-the-road driving test and a car-following test.

Detailed description

The study shall be conducted according to a three-way, double-blind, placebo and active controlled crossover design. Treatment groups are identified as follows. * Rupatadine * Hydroxyzine * Placebo

Conditions

Interventions

TypeNameDescription
DRUGRupatadine
DRUGHydroxyzine
DRUGPlacebo

Timeline

Start date
2005-05-01
Completion
2005-11-01
First posted
2005-09-13
Last updated
2006-10-20

Locations

1 site across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT00162786. Inclusion in this directory is not an endorsement.