- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03932110
Metabolic Syndrome in Psoriasis and Psoriatic Arthritis and Correlation With Serum Omentin and Visfatin Levels
June 14, 2019 updated by: Deniz Dağdelen, Istanbul Medeniyet University
The Prevalence of Metabolic Syndrome in Patients With Psoriasis and Psoriatic Arthritis and Its Correlation With Disease Severity and Serum Omentin-1 and Visfatin Levels
In this study, the prevalence of metabolic syndrome in psoriatic and psoriatic arthritis patients as well as the parameters of metabolic syndrome will be examined.
At the same time, the levels of omentin and visfatin adipokines associated with metabolic syndrome and obesity will be measured by measuring the disease severity (by PASI psoriasis, clinical activity score for psoriatic arthritis).
The patients who accepted to participate in the study , who were admitted to the dermatology outpatient clinic were included in the study.
For the blood tests required after the examination, 2 tubes of blood will be taken for the measurement of omentin and visfatin.
80 psoriasis, 40 psoriatic arthritis and 60 healthy volunteers were planned to be studied.
AHA / NHLBI, 2005 (revised ATP III criteria) criterion for the diagnosis of metabolic syndrome will be used.
Omentin and visfatin levels are compared with the severity of the disease for psoriasis and psoriatic arthritis, and it will be examined whether it is proinflammatory or antiinflammatory.
Study Overview
Status
Completed
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
180
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Istanbul, Turkey, 34722
- Istanbul Medeniyet University
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Istanbul, Turkey, 34722
- Istanbul Medeniyet University, Department of dermatology
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 80 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Description
Inclusion Criteria:
- Patients followed up for psoriasis and psoriatic arthritis in dermatology and rheumatology clinic
- Patients older than 18 years
- Patients who accept dermatological and rheumatic examination
- Patients not receiving systemic treatment related to the disease in the last 1 month
Exclusion Criteria:
- Patients with autoimmune and rheumatic diseases other than psoriasis and psoriatic arthritis
- Patients under 18 years
- Patients who do not accept dermatological and rheumatic examination Patients receiving systemic therapy for the last 1 month pregnant and nursing moms
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: DIAGNOSTIC
- Allocation: NON_RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
OTHER: psoriasis vulgaris,
patients who have only psoriasis vulgaris
|
diagnostic blood test
|
OTHER: psoriatic arthritis
patients who have psoriatic arthritis
|
diagnostic blood test
|
OTHER: healthy control
healthy people
|
diagnostic blood test
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
omentin
Time Frame: 6 months
|
Omentin (omentin 1-2) is a specific protein that consists of amino acids released from vascular vessels
|
6 months
|
visfatin
Time Frame: 6 months
|
Visfatin is an insulin-like protein that binds to insulin receptors produced mostly from visceral fatty tissue.
|
6 months
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
April 15, 2019
Primary Completion (ACTUAL)
June 1, 2019
Study Completion (ACTUAL)
June 14, 2019
Study Registration Dates
First Submitted
April 24, 2019
First Submitted That Met QC Criteria
April 26, 2019
First Posted (ACTUAL)
April 30, 2019
Study Record Updates
Last Update Posted (ACTUAL)
June 17, 2019
Last Update Submitted That Met QC Criteria
June 14, 2019
Last Verified
June 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
- Pathologic Processes
- Glucose Metabolism Disorders
- Metabolic Diseases
- Skin Diseases
- Disease
- Joint Diseases
- Musculoskeletal Diseases
- Skin Diseases, Papulosquamous
- Insulin Resistance
- Hyperinsulinism
- Spinal Diseases
- Bone Diseases
- Spondylarthropathies
- Spondylarthritis
- Spondylitis
- Syndrome
- Arthritis
- Psoriasis
- Metabolic Syndrome
- Arthritis, Psoriatic
Other Study ID Numbers
- DDagdelen
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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