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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06370221
Other study ID # psoriatic Arthritis
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date June 1, 2024
Est. completion date December 30, 2024

Study information

Verified date April 2024
Source Egymedicalpedia
Contact Eisa Hegazy, Professor
Phone +201094337795
Email eisa_mohamed4152@med.svu.edu.eg
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Psoriasis is one of the most common immunemediated chronic inflammatory skin disorders.


Description:

Psoriasis is one of the most common immunemediated chronic inflammatory skin disorders. Beside genetic factors, several environmental factors such as injuries, infections, stress, drugs, and immune defect take part in autoimmune pathogenesis of the disease. In addition, it has been reported that some hormones may also have a role in the pathogenesis of psoriasis, due to their effects on keratinocytes proliferation. Studies revealed that sex hormones manifest a variety of biological and immunological effects in the skin which modulate the natural course of psoriasis. Approximately 20-30% of patients with psoriasis may also have psoriatic arthritis, which often causes significant musculoskeletal pain that significantly impairs quality of life (QoL). Although sexual dysfunction is a common complaint, affecting 30 to 70% of psoriasis patients, few studies have analyzed the impact of psoriasis and psoriatic arthritis on quality of sexual life.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 180
Est. completion date December 30, 2024
Est. primary completion date December 20, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 40 Years
Eligibility Inclusion Criteria: - The study will focuses on the relationship between the FSD and PsA; - The healthy controls will derive from a population within the same geographic area and ethnic background as PsA; - Used the same questionnaires/instruments of FSFI to diagnose FSD Exclusion Criteria: - pregnancy, - breastfeeding - being sexually inactive - having a partner with sexual dysfunction, - refusing to participate, or - being unable to read - Females with any sexual transmitted disease

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
The effect of psoriatic Arthritis
to assess the frequency rates of sexual problems and associated factors in a cohort of married females with Psoriatic arthritis, and to investigate the correlation between sex hormones profile ( estrogen and progesterone level) and female sexual function in Psoriatic arthritis patients.

Locations

Country Name City State
Egypt Qena Hospital Qina

Sponsors (1)

Lead Sponsor Collaborator
Egymedicalpedia

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Primary Evaluation of female sexual function To identify and understand the mechanisms of sexual problems in Psoriatic arthritis Patients in Qena university hospital. 6 months
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