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Effects of Primary Sjögren's Syndrome on Female Genitalia and Sexual Functions

NCT04816370 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 68

Last updated 2021-03-25

No results posted yet for this study

Summary

A total of 68 women with pSS and 135 healthy female patients were included in the study. All women in the study and control groups were evaluated gynecologically, and genital findings during the examination and variables related to pSS were recorded. Women's sexual functions were evaluated with the Female Sexual Function Index (FSFI) and quality of life was evaluated using the Health Status Questionnaire-Short Form 36.

Conditions

  • Primary Sjögren Syndrome

Interventions

DIAGNOSTIC_TEST

FSFI

2 group and 2 subgroup

Sponsors & Collaborators

  • Ankara Education and Research Hospital

    lead OTHER_GOV

Principal Investigators

  • Murat Gözüküçük · Ankara Training and Research Hospital

Study Design

Allocation
RANDOMIZED
Purpose
SCREENING
Masking
SINGLE
Model
CROSSOVER

Eligibility

Min Age
20 Years
Max Age
70 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2015-07-02
Primary Completion
2020-11-15
Completion
2021-01-25

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04816370 on ClinicalTrials.gov