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NCT04816370

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

Completed NA Last updated 25 March 2021
What this trial tests

NA trial testing FSFI in Primary Sjögren Syndrome in 68 participants. Completed in 25 January 2021.

Timeline
2 July 2015
Primary endpoint
15 November 2020
25 January 2021

Quick facts

Lead sponsorAnkara Education and Research Hospital
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingsingle
Primary purposescreening
Enrollment68
Start date2 July 2015
Primary completion15 November 2020
Estimated completion25 January 2021
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Ankara Education and Research Hospital

Who can join

Adults 20 to 70, female only, with Primary Sjögren Syndrome. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

Verify or expand the search:

Other trials of FSFI

Trials testing the same drug.

Other recruiting trials for Primary Sjögren Syndrome

Currently open trials in the same condition.

Other Ankara Education and Research Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04816370.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing