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Body PSOriasis: Long-term Relapse CONTROL

Body PSOriasis: Long-term Relapse Control in Patients With Psoriasis Vulgaris in Daily Clinical Practice of Russian Dermatologists.

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03402828
Acronym
PSO-CONTROL
Enrollment
764
Registered
2018-01-18
Start date
2018-06-11
Completion date
2020-05-15
Last updated
2021-03-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Psoriasis Vulgaris

Keywords

Topicals, Long-term

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.

Interventions

DRUGAny topical drug treatment

Any treatment strategy used to prevent relapse of psoriasis symptoms

Sponsors

LEO Pharma
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frameDescription
Time of relapseUp to 52 weeksLength of relapse free period after start of maintenance strategy

Secondary

MeasureTime frameDescription
Dermatology Life Quality IndexUp to 52 weeksStandard QoL measure within dermatology
PGA (physician's global assessment of symptoms)Up to 52 weeks5-point verbal rating scale
PsGA (patient's global assessment of symptoms)Up to 52 weeks5-point verbal rating scale

Countries

Russia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026