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Study identifier: NCT06918873 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Quality of Life During Different Regimens of Combined Hormonal Contraceptives in Women of Reproductive Age

Condition: Hormonal Contraception  ·  Sponsor: Fondazione IRCCS Policlinico San Matteo di Pavia

PhaseN/A
Planned participants400
Who can joinFemale, 18 Years to 40 Years
Healthy volunteersNo

About this study

The aim of the present study is to investigate the psychosexual effects of combined hormonal contraception regimens, comparing them in terms of estrogen type and dosage, hormonal combination regimen and different routes of administration, in women seeking a hormonal contraception method to prevent unwanted pregnancies. In particular, the study focuses on the incidence of mood disorders and sexual dysfunctions associated with distress in the entire study population using combined hormonal contraception. It will also examine the incidence of these conditions under the influence of specific combined hormonal contraceptives, as well as whether different types of progestins and the route of administration (oral, vaginal or transdermal) may affect the occurrence of mood disorders and sexual dysfunctions.

This description comes directly from the study's public registry record.

Talk to the study team

Rossella Nappi, MD  ·  +390382503325  ·  r.nappi@smatteo.pv.it

Always discuss trial participation with your own doctor first.

Locations (1)

Fondazione IRCCS Policlinico San Matteo, SSD Ostetricia e Ginecologia 2 - Riproduzione e Procreazione Medicalmente AssistitaPavia, Pavia, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06918873