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NCT07259525Worth exploringNot yet recruiting

Escitalopram levels in women before and after menopause

Therapeutic Drug Monitoring (TDM)MenopauseDepression - Major Depressive DisorderGeneral Anxiety Disorder

Part of Mental health clinical trials.

This study looks at how the body processes escitalopram (an antidepressant) differently in women before and after menopause. It aims to help doctors understand if dosing should be adjusted based on menopausal status.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
94 people
Ages
40 years to 60 years
Study type
Observational

Who can take part

  • Women aged 40 to 60
  • Diagnosed with depression or generalized anxiety disorder
  • Currently taking escitalopram for at least a month
  • Either have regular periods (and are in the second half of your cycle) or have not had a period for at least a year
  • Not taking certain other medications or hormone treatments (like birth control pills or hormone replacement therapy)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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