Escitalopram Plasma Concentrations in Premenopausal and Postmenopausal Women

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age40-60
SponsorEskisehir Osmangazi University

About this trial

This observational cross-sectional case-control study aims to evaluate the effects of menopausal status on escitalopram metabolism in women. The study will include premenopausal and menopausal women aged 40-60 years who are currently receiving escitalopram treatment and have applied to the Psychiatry Clinic of Eskişehir Osmangazi University. The study aims to identify pharmacokinetic differences associated with hormonal status and to investigate their potential clinical implications. Findings from this research are expected to contribute to the development of evidence-based, individualized treatment strategies for women in menopausal transition.

Eligibility criteria

Qualifiers

Aged 40 years or older and 60 years or younger

Diagnosed with major depressive disorder and/or generalized anxiety disorder by an independent psychiatrist (not a member of the research team)

Prescribed escitalopram treatment by an independent psychiatrist (not a member of the research team)

Receiving escitalopram treatment for at least one month and on a stable dose for at least one week

Disqualifiers

Diagnosis of intellectual disability, dementia, psychotic disorders, schizoaffective disorder, or bipolar disorder

Alcohol or substance use disorder

Diagnosis of hepatic failure, renal failure, or cardiac failure

Severe malnutrition

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

94 Participants
are grouped into 2 trial groups

Sponsors and collaborators

Eskisehir Osmangazi University

Lead sponsor

The Scientific and Technological Research Council of Turkey

Collaborator