Clinical Trials Directory

Trials / Withdrawn

WithdrawnNCT01125761

Efficacy and Safety of the Association Drugs in Patients With Allergic Dermatitis

Efficacy and Safety of the Association of Dexamethasone 0.5 mg + Clemastine Fumarate 1 mg When Compared to Dexamethasone 0.5 mg in Patients With Allergic Dermatitis

Status
Withdrawn
Phase
Phase 3
Study type
Interventional
Enrollment
0 (actual)
Sponsor
Azidus Brasil · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Considering the pathogenesis of several allergic skin diseases to be investigated in this study as well as the pharmacodynamic mechanisms of the association of dexamethasone and clemastine fumarate, it is believed that the components of topical medication may act synergistically in the reduction of signs and symptoms of the diseases in question. Therefore it is expected that the association promotes results significantly superior to dexamethasone alone.

Conditions

Interventions

TypeNameDescription
DRUGdexamethasone 0.5 mg and 1.0 mg clemastine creamThe treatment should be administered every 12 hours so that a thin layer is applied on the lesions, for 14 days.
DRUGDexamethasone 0,5 mg creamThe treatment should be administered every 12 hours so that a thin layer is applied on the lesions, for 14 days.

Timeline

Start date
2010-11-01
Primary completion
2010-11-01
Completion
2010-11-01
First posted
2010-05-18
Last updated
2022-11-03

Locations

2 sites across 1 country: Brazil

Source: ClinicalTrials.gov record NCT01125761. Inclusion in this directory is not an endorsement.