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Body PSOriasis: Long-term Relapse CONTROL

Completed
Conditions
Psoriasis Vulgaris
Registration Number
NCT03402828
Lead Sponsor
LEO Pharma
Brief Summary

This non-interventional study of real-life clinical practice strategies for long-term relapse control in patients with psoriasis vulgaris is planned to enroll 650 adult patients from 60-100 Russian dermatology sites and follow the patients for up to 52 weeks. The study will map actual strategies and focus on patients' and dermatologists' experience with the different topicals used, including unspecified products with and without active drugs.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
764
Inclusion Criteria
  • Patients planned to receive topical treatment of any kind to prevent relapse of symptoms
  • Written informed consent
Exclusion Criteria
  • Contraindications to selected treatment
  • Ongoing systemic treatment of psoriasis with steroids, anti-inflammatory drugs or phototherapy

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Time of relapseUp to 52 weeks

Length of relapse free period after start of maintenance strategy

Secondary Outcome Measures
NameTimeMethod
Dermatology Life Quality IndexUp to 52 weeks

Standard QoL measure within dermatology

PGA (physician's global assessment of symptoms)Up to 52 weeks

5-point verbal rating scale

PsGA (patient's global assessment of symptoms)Up to 52 weeks

5-point verbal rating scale

Trial Locations

Locations (1)

The State Autonomous Foundation of Public Health "Republic Clinical Dermatovenereological Dispensary" of the Republic of Tatarstan

🇷🇺

Kazan, Tatarstan, Russian Federation

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