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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 50 mcg/g plus betamethasone 0.5 mg/g (as dipropionate) gel is safe and more effective than betamethasone 0.5 mg/g (as dipropionate) in the gel vehicle, calcipotriol 50 mcg/g in the gel vehicle or the gel vehicle used alone in patients with scalp psoriasis.

The primary outcome is the proportion of patients with absence of disease or very mild disease after 8 weeks of treatment.


Clinical Trial Description

n/a


Study Design

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


Related Conditions & MeSH terms


NCT number NCT00216827
Study type Interventional
Source LEO Pharma
Contact
Status Completed
Phase Phase 3
Start date November 2004
Completion date September 2005

See also
  Status Clinical Trial Phase
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Completed NCT05105139 - Study to Evaluate the Safety of Sebryl® and Sebryl Plus® in Seborrheic Dermatitis and Psoriasis of Scalp
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
Recruiting NCT05938361 - Efficacy of Tildrakizumab in Difficult-to-treat Areas in Psoriasis
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