Clinical Trials Directory

Trials / Completed

CompletedNCT00546000

Cutivate Lotion HPA Axis Pediatric Study

A Multi-Center, Open-Label Study to Evaluate the Effect of ALTANA Inc's Cutivate (Fluticasone Propionate) Lotion 0.05% on the Hypothalmic Pituitary Adrenal (HPA) Axis in the Treatment of Atopic Dermatitis in a Pediatric Population

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
56 (actual)
Sponsor
Fougera Pharmaceuticals Inc. · Industry
Sex
All
Age
3 Months – 12 Months
Healthy volunteers
Not accepted

Summary

A multi-center, open-label, Phase IV, unblinded study using Cutivate (fluticasone propionate, 0.05%)lotion and it's possible effects on the HPA axis of infants diagnosed with atopic dermatitis.

Conditions

Interventions

TypeNameDescription
DRUGFluticasone propionate 0.05% lotionDaily applications

Timeline

Start date
2007-07-01
Primary completion
2008-12-01
Completion
2008-12-01
First posted
2007-10-18
Last updated
2014-07-24
Results posted
2014-07-24

Locations

10 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT00546000. Inclusion in this directory is not an endorsement.

Cutivate Lotion HPA Axis Pediatric Study (NCT00546000) · Clinical Trials Directory