Clin2
NCT07259525Possibly a fitNot yet recruiting

Escitalopram levels in premenopausal and postmenopausal women

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

Part of Mental health clinical trials.

This study measures how the antidepressant escitalopram builds up in the blood of women before and after menopause. It aims to see if hormone changes affect drug levels, which could help doctors adjust doses for better treatment.

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

  • You are a woman between 40 and 60 years old.
  • You have been diagnosed with major depression or generalized anxiety by a doctor not in the research team.
  • You have been taking the antidepressant escitalopram for at least one month and on the same dose for at least one week.
  • You are willing to join and sign a consent form.
  • If you are postmenopausal: you have not had a period for at least one year.
  • If you are premenopausal: you have regular periods and are in the luteal phase (14 days after ovulation).

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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