Evaluation of the Presence of Enthesitis in Patients With Acne Vulgaris
Overview
Acne vulgaris is an inflammatory disease of the pilosebaceous unit, affecting about 85% of the young population. In the studies p. acne is a potent stimulator of the release of IFN-gamma (IFN-)) and IL-17 from CD4 + T cells, and the presence of IL-17 + cells in the perifollicular infiltrate has been shown in biopsies of inflammatory acne lesions. Therefore, acne is thought to be a Th17-related disease (1). This study was aimed to evaluate the presence of enthesitis in patients with acne vulgaris.
Study Type
- Study Type: Observational
- Study Design
- Time Perspective: Cross-Sectional
- Study Primary Completion Date: April 1, 2020
Detailed Description
Patients with acne vulgaris and healthy controls aged between 18-25 who admitted to Hitit University Erol Olcok Education and Research Hostpital Dermatology policlinic will be icluded. Patients with rheumatic, neurological diseases, history of trauma and previous fractures will be excluded from the study. After all the participants were evaluated by the dermatologist and demographic data will be recorded, the participants will be examined by the physical medicine and rehabilitation specialist and the short form-36 (sf-36), hospital anxiety and depression scale will be completed. Bilateral lower extremity tendon thicknesses and the presence of erosion, bursitis, etc. will be evaluated according to the criteria of Guess (Glasgow Ultrasound Enthesitis Scoring System) and Guess score will be determined for all participants. A total of 48 participants, 24 patients with acne vulgaris and 24 healthy controls, will be included in the study (2).
Interventions
- Diagnostic Test: ultrasonography
- all participants will be determined by ultrasonography.
Arms, Groups and Cohorts
- Patients with acne vulgaris
- patients with acne vulgaris aged between 18-25 year
- Healthy controls
- healthy controls aged between 18-25 year
Clinical Trial Outcome Measures
Primary Measures
- patellar tendon thicknesses of patients with acne vulgaris and healthy controls
- Time Frame: 3 months
- Ashilles tendon thicknesses of patients with acne vulgaris and healthy controls
- Time Frame: 3 months
Participating in This Clinical Trial
Inclusion Criteira:
- Patients with acne vulgaris and healthy controls aged between 18-25 Exclusion Criteria:
- Participants with rheumatic and neurologic disease, history of trauma ,
Gender Eligibility: Female
Minimum Age: 18 Years
Maximum Age: 25 Years
Are Healthy Volunteers Accepted: Accepts Healthy Volunteers
Investigator Details
- Lead Sponsor
- Erol Olcok Corum Training and Research Hospital
- Provider of Information About this Clinical Study
- Principal Investigator: Dilek Eker Büyükşireci, Specialist doctor – Erol Olcok Corum Training and Research Hospital
- Overall Contact(s)
- Dilek E Büyükşireci, +905439196253, dilekeker55@gmail.com
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