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Clinical Trial Summary

The purpose of this study is to evaluate whether once daily treatment for up to 8 weeks of calcipotriol plus betamethasone dipropionate gel is more effective than twice daily treatment of calcipotriol scalp solution in patients with scalp psoriasis. The primary outcome is patients with clear or minimal disease after 8 weeks treatment.

Further the occurrence of relapse and rebound after end of treatment in patients with clear or minimal disease will be investigated.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00243464
Study type Interventional
Source LEO Pharma
Contact
Status Completed
Phase Phase 3
Start date September 2005
Completion date May 2006

See also
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Completed NCT00216827 - Efficacy and Safety of Calcipotriol Plus Betamethasone Gel in the Treatment of Scalp Psoriasis Phase 3
Recruiting NCT04099979 - A Pilot Study to Explore the Role of Gut Flora in Psoriasis
Not yet recruiting NCT03553433 - Apremilast Treatment for Pruritus and Quality of Life in Scalp Psoriasis Phase 4
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Recruiting NCT05858632 - Immune Spatial Features of Guselkumab Cutaneous Response Phase 4
Completed NCT00216879 - Efficacy and Safety of Calcipotriol Plus Betamethasone Dipropionate Gel for up to a Year in Scalp Psoriasis Phase 3
Completed NCT00216840 - Efficacy and Safety of Calcipotriol Plus Betamethasone Dipropionate Gel in Scalp Psoriasis Phase 3