Assessment of the Improvement in Cognitive Levels of Postmenopausal Depression Patients by Estrogen

NARecruitingINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

May 12, 2023

Primary Completion Date

December 30, 2024

Study Completion Date

December 30, 2024

Conditions
Postmenopausal DepressionEstrogen
Interventions
DRUG

Fematon (estradiol/estradiol-norethindrone acetate combination tablet package)+SSRIs

In the combination group, eligible subjects will receive 1 tablet/day of estradiol/estradiol-norethindrone acetate combination tablet for 8 weeks. The estradiol/estradiol-norethindrone acetate combination tablet will be taken orally before bedtime, 1 tablet/day (trade name: Fematon, Abbott Laboratories, USA, this product is a combination package, with estradiol 1 mg in the first 14 days of each treatment cycle, and estradiol 1 mg and norethindrone acetate 10 mg in the last 14 days of each treatment cycle). This study uses SSRIs class drugs, including fluoxetine, paroxetine, fluvoxamine, sertraline, citalopram, and escitalopram.

DRUG

SSRIs

This study uses SSRIs class drugs, including fluoxetine, paroxetine, fluvoxamine, sertraline, citalopram, and escitalopram, with no specific restrictions on the type of drugs. During the study, medication doses will be quantitatively adjusted based on the results of each visit assessment combined with drug concentrations.

Trial Locations (1)

Unknown

RECRUITING

Beijing Anding Hospital Affiliated to Capital Medical University, Beijing

All Listed Sponsors
lead

Xiao Wang

OTHER