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Clinical Study of PET/CT and Association With Metabolic Syndrome/Depressive Symptoms in Psoriasis

Phase 0 Clinical Study of PET/CT and Association With Metabolic Syndrome/Depressive Symptoms in Psoriasis

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01661127
Enrollment
10
Registered
2012-08-09
Start date
2012-06-30
Completion date
2015-12-31
Last updated
2014-11-04

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

Conditions

Depression, Metabolic Syndrome, Psoriasis

Brief summary

Psoriasis is associated with increases in markers of inflammation in the skin and blood and increasingly is thought to be a systemic inflammatory disease and risk factor for incident diabetes mellitus, myocardial infarction, stroke, and premature cardiovascular death. Furthermore, it is important for clinicians to be aware that psoriasis can have a substantial emotional impact on an individual, which is not necessarily related to the extent of skin disease. FDG-PET/CT represents an innovative approach to studying systemic inflammation in a manner that is sensitive, quantifiable, and anatomically localizable. Also, recent study show that chronic disease such as end stage renal disease with depressive symptoms have decreased cerebral glucose metabolism in several brain areas in F-18-FDG PET/CT. So this protocol was designed to evaluate usefulness of PET/CT to detect systemic inflammation and abnormality of cerebral glucose metabolism and association with metabolic syndrome/major depressive symptoms in patients with psoriasis.

Detailed description

10 Patients with psoriasis 1. Evaluate PASI score 2. Evaluate comorbidity with metabolic syndrome * Body mass index(BMI) * Checking blood pressure * Checking blood sugar * Smoking and drinking history * Checking blood cholesterol level * Risk factors of cardiovascular disease 3. PET/CT for measuring the extent and site of psoriasis with inflammation

Interventions

None listed

Sponsors

Pusan National University Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* Histological diagnosis of plaque type psoriasis * at least 18 years old

Exclusion criteria

* those who cannot understand questionnaire * those who take antidepressant

Design outcomes

Primary

MeasureTime frame
Beck depression inventory scoring and Korean Hamilton depression scale scoringDay 0 and 28 weeks later

Secondary

MeasureTime frame
Brain glucose uptake using PET/CTDay 0 and 28 weeks later

Countries

South Korea

Contacts

Primary ContactByung-Soo Kim, Ph D.
dockbs@pusan.ac.kr82-51-240-7338

Outcome results

None listed

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