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Clinical Trial Summary

The purpose of the study is to evaluate whether once daily topical 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 and calcipotriol 50 mcg/g in the gel vehicle in patients with scalp psoriasis.

The primary response criterion is the number of patients with absence of disease and 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 NCT00216840
Study type Interventional
Source LEO Pharma
Contact
Status Completed
Phase Phase 3
Start date December 2004
Completion date September 2005

See also
  Status Clinical Trial Phase
Completed NCT00243464 - Efficacy of Calcipotriol Plus Betamethasone Gel Versus Calcipotriol Scalp Solution in Scalp Psoriasis Phase 3
Recruiting NCT05144165 - Systemic Treatment of Moderate-to-severe Psoriasis in Adults: Update of the French Guidelines
Completed NCT05105139 - Study to Evaluate the Safety of Sebryl® and Sebryl Plus® in Seborrheic Dermatitis and Psoriasis of Scalp
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
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