A Clinical Study of Subclinical Enthesitis and Synovitis in Patients With Vulgaris Psoriasis

NCT ID: NCT02339636

Last Updated: 2015-01-15

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

UNKNOWN

Total Enrollment

200 participants

Study Classification

OBSERVATIONAL

Study Start Date

2015-03-31

Study Completion Date

2016-12-31

Brief Summary

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A clinical study of subclinical enthesitis and synovitis in patients with vulgaris psoriasis

Detailed Description

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A total of 100 patients with vulgaris psoriasis and 100 age-matched controls with other skin diseases, all without musculoskeletal diseases, will be recruited. They will undergo dermatological assessment and a blinded PDUS evaluation. Clinical assessment included demographics, severity of psoriasis, musculoskeletal clinical examination and sport activities. PDUS evaluation consisted of the detection of grey scale (GS) synovitis and synovial PD signal in joints of extremities, GS enthesopathy and entheseal PD signal in entheses of lower limbs.

Conditions

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Vulgaris Psoriasis

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

RETROSPECTIVE

Study Groups

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case group

100 patients with vulgaris psoriasi without arthritis

PDUS examination

Intervention Type OTHER

control group

100 age-matched patients with other skin diseases without arthritis

PDUS examination

Intervention Type OTHER

Interventions

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PDUS examination

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* age≥18years
* patients with vulgaris psoriasis(dur
* patients with other skin diseases without musculoskeletal disorders
* no joint involvement and no clinical symptoms and signs of enthesitis and synovitis

Exclusion Criteria

* BMI≥24
* have history of gout or arthritis or peripheral neurological disease of lower extremity or trauma
* have received any systemic therapy(i.e.NSAIDs, corticosteroids, immunosuppressants, retinoids or biological agents) in 3 months
* pregnant or breast-feeding
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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The 306 Hospital of People's Liberation Army

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Jianjun Liu, M.D.

Role: PRINCIPAL_INVESTIGATOR

The 306 Hospital of People's Liberation Army

Locations

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306 Hospital of PLA

Beijing, , China

Site Status

Countries

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China

Facility Contacts

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jianjun liu, MD

Role: primary

Other Identifiers

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306PLA-002

Identifier Type: -

Identifier Source: org_study_id

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