Comparison of the Frequency of Subclinic Synovitis in the Distal Interphalangeal Joints of the Hand in Psoriasis Patients

Sponsor
Ufuk University (Other)
Overall Status
Completed
CT.gov ID
NCT04750993
Collaborator
(none)
56
1
8
7

Study Details

Study Description

Brief Summary

In this cross-sectional study, it was planned to compare the frequency of subclinical synovitis in the distal interphalangeal joints of the hands in psoriasis patients. 28 patients followed up by the Dermatology Department with a diagnosis of psoriasis and referred to us and 28 healthy volunteers were included in the study. Participants' age, gender, body mass index (BMI), year of psoriasis diagnosis, treatments they received, and comorbid diseases were recorded as demographic information. Psoriasis Area and Severity Index (PASI) and Nail Psoriasis Severity Index (NAPSI) were calculated by a dermatologist.

Tenderness in the distal interphalangeal joints of both hands was evaluated by palpation.

Subsequently, the presence of ultrasonographic synovitis findings of the participants was examined by a physician who was experienced in musculoskeletal ultrasonography and was blind to clinical evaluations. Scoring was done with the EULAR GS / PD joint scoring system and EULAR-OMERACT composite scoring system. The scores of the most affected joint were used in statistical analysis. Comparisons were made between psoriasis and control groups in terms of scores. Relationships between variables in the psoriasis group were examined.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: musculoskeletal ultrasonography

Study Design

Study Type:
Observational
Actual Enrollment :
56 participants
Observational Model:
Other
Time Perspective:
Cross-Sectional
Official Title:
Comparison of the Frequency of Subclinic Synovitis in the Distal Interphalangeal Joints of the Hand in Psoriasis Patients
Actual Study Start Date :
Oct 1, 2014
Actual Primary Completion Date :
Jun 1, 2015
Actual Study Completion Date :
Jun 1, 2015

Outcome Measures

Primary Outcome Measures

  1. GS/PD score [8 month]

    Intaarticular fluid (0 = absent, 1 = present), synovial hypertrophy (0 = absent, 1 = mild, 2 = moderate, 3 = severe), bone erosion (0 = absent, 1 = 2 erosion, 2 = More than 2 erosion), surrounding soft tissue swelling (0 = absent, 1 = mild, 2 = moderate) with gray scale; the presence of blood flow in the area with synovial proliferation with power Doppler (0 = no signal, 1 = less signal in one vessel, 2 = moderate signal at vascular intersections, 3 = intense signal on more than half of the joint surface) are evaluated and scored. GS and PD scores of the joint with the greatest involvement are used in statistical analysis.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:

For patient group

  1. Being over the age of 18

  2. Being followed up by the Dermatology Department with a diagnosis of psoriasis and receiving topical or systemic treatment for this

  3. Absence of clinically detected signs of arthritis

  4. Absence of serious trauma, surgical intervention or injection in the joint areas to be evaluated.

  5. Absence of any known inflammatory rheumatic disease For control group

1.> 18 years old 2. Absence of clinically detected signs of arthritis 3.Lack of clinical signs suggestive of psoriasis

Exclusion Criteria:

For patient group

  1. To be <18 years old

  2. Clinically detected evidence of arthritis

  3. History of serious trauma, surgical intervention or injection in the joint areas to be evaluated

  4. Having a known inflammatory rheumatic disease For control group

  5. To be <18 years old 2. Having clinical signs suggestive of psoriasis 3. Having clinically detectable signs of arthritis 4. History of known inflammatory disease, severe trauma in the joint areas to be evaluated, surgical intervention, injection

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ufuk University Ankara Çankaya Turkey 06520

Sponsors and Collaborators

  • Ufuk University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Elzem Bolkan Günaydın, Lecturer Doctor, Ufuk University
ClinicalTrials.gov Identifier:
NCT04750993
Other Study ID Numbers:
  • 465/Gazi University
First Posted:
Feb 11, 2021
Last Update Posted:
Feb 11, 2021
Last Verified:
Feb 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 11, 2021