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NCT02627989: Ointment TS-AD

An Observational Study Investigating the Treatment Satisfaction of Atopic Dermatitis Patients Who Have Switched to Ointment (W/O Emulsion) Formulation of Very Strong Class Topical Corticosteroids

Completed Last updated 1 April 2020
What this trial tests

trial testing Diflucortolone valerate (Nerisona) in Dermatitis, Atopic in 55 participants. Completed in 17 January 2017.

Timeline
10 December 2015
Primary endpoint
17 November 2016
17 January 2017

Quick facts

Lead sponsorLEO Pharma
StatusCompleted
Study typeOBSERVATIONAL
Enrollment55
Start date10 December 2015
Primary completion17 November 2016
Estimated completion17 January 2017
Sites1 location across Japan

Drugs / interventions tested

Conditions studied

Sponsor

LEO Pharma — full company profile →

Who can join

20 and older, any sex, with Dermatitis, Atopic. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study intends to investigate patient satisfaction of treatment with Ointment (W/O emulsion) formulations of Potency Class II topical corticosteroids (TCs) for atopic dermatitis (AD) patients in Japan. Objectives include measuring patient satisfaction, treatment adherence, itchiness, and AD severity scores.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other recruiting trials for Dermatitis, Atopic

Currently open trials in the same condition.

Other LEO Pharma trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02627989.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing