Cardiovascular Risk Predictors in Patients With Psoriasis

NCT ID: NCT05200598

Last Updated: 2024-10-08

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-10-01

Study Completion Date

2024-09-01

Brief Summary

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The investigators are planning to find the right modification of traditionally used risk scores (PASI, DLQI) in patients with psoriasis of different severity to guide the treatment that could potentially extend life, improve cardiovascular outcomes and quality of life in patients with psoriasis and cardiovascular risk factors in a prospective observational study. The traditionally excluded groups of older patients with diabetes mellitus, decreased kidney function and those with potentially worse prognosis are going to be included in the study. As it's known, the number of those patients is on the rise each year and require a close attention of multidisciplinary teams.

Detailed Description

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Conditions

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Psoriasis Cardiovascular Diseases

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Mild psoriasis

No interventions assigned to this group

Moderate psoriasis

No interventions assigned to this group

Severe psoriasis

No interventions assigned to this group

Patients without psoriasis

No interventions assigned to this group

Eligibility Criteria

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Inclusion Criteria

* Age over 18 years
* Written informed consent of the patient to participate in the study

Exclusion Criteria

* Age under 18
* Pregnancy, lactation
* Very high cardiovascular risk
* Life-threatening, independently influencing prognosis and disabling diseases,
* Mental disorders that do not allow to give informed consent or answer questions adequately
* Refuse of the patient to participate in the study
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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I.M. Sechenov First Moscow State Medical University

OTHER

Sponsor Role lead

Responsible Party

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Olga Mironova

Associate Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Olga Mironova, MD, PhD

Role: PRINCIPAL_INVESTIGATOR

Sechenov University

Locations

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University Clinical Hospital #2

Moscow, , Russia

Site Status

Countries

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Russia

Other Identifiers

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22-21

Identifier Type: -

Identifier Source: org_study_id

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