Citalopram in Treating Postmenopausal Women With Hot Flashes | NCT00363909 | Trialant

Citalopram in Treating Postmenopausal Women With Hot Flashes | NCT00363909 | Trialant

Official Title: Phase III Randomized, Double-Blind, Placebo-Controlled Evaluation of Citalopram for the Treatment of Hot Flashes
Brief Summary: RATIONALE: Citalopram may help relieve hot flashes in women who had or have not had breast cancer. It is not yet known which dose of citalopram is more effective in treating hot flashes in postmenopausal women.

PURPOSE: This randomized phase III trial is studying three different doses of citalopram to compare how well they work in treating postmenopausal women with hot flashes.
Detailed Description: OBJECTIVES:

Primary

Evaluate the efficacy of three different doses of citalopram hydrobromide on hot flash scores in postmenopausal women with a history of breast cancer or in postmenopausal women who do not wish to take estrogen replacement therapy for fear of increased risk of breast cancer.

Secondary

Compare the side effect profile of these regimens in these patients.

Compare the effects of these regimens on the secondary outcome of mood and interference with activities from hot flashes.

Determine if CYP2C19 and CYP2D6 polymorphisms predict efficacy of various doses of citalopram hydrobromide.

OUTLINE: This is a randomized, double-blind, placebo-controlled, multicenter study. Patients are stratified according to age (18-49 years vs ≥ 50 years), tamoxifen (yes vs no), selective estrogen-receptor modulators (SERMs) (yes vs no), aromatase inhibitors (yes vs no), duration of hot flashes (< 9 months vs ≥ 9 months), and frequency of hot flashes per day (< 4 vs 4-9 vs ≥ 10). Patients are randomized to 1 of 4 treatment arms.

Arm I (low-dose citalopram hydrobromide): Patients receive 1 tablet of oral citalopram once daily in weeks 2-7.

Arm II (medium-dose citalopram hydrobromide): Patients receive 1 tablet of oral citalopram once daily in week 2 and 2 tablets once daily in weeks 3-7.

Arm III (high-dose citalopram hydrobromide): Patients receive 1 tablet of oral citalopram once daily in week 2, 2 tablets once daily in week 3, and 3 tablets once daily in weeks 4-7.

Arm IV (placebo): Patients receive 1-3 placebo tablets once daily in weeks 2-7. All patients complete a diary of hot flash incidence in weeks 1-7 and undergo blood collection periodically during study treatment for translational research studies.

A Symptom Experience diary is completed weekly and Profile of Mood States and Hot Flash-Related Interference Scale questionnaires are completed at baseline and in week 7.

Ages Eligible for Study: Adult (18-64)Older Adult (65+)
Sexes Eligible for Study: Female
Accepts Healthy Volunteers: No
Eligibility Criteria: DISEASE CHARACTERISTICS:

Must meet 1 of the following criteria:

History of breast cancer

No current malignant disease

No history of breast cancer and refused estrogen replacement therapy due to perceived increased risk of breast cancer

Bothersome hot flashes, defined as hot flashes ≥ 14 times/week and of sufficient severity to make the patient desire therapeutic intervention

Presence of hot flashes ≥ 1 month prior to study entry

Hormone receptor status not specified

PATIENT CHARACTERISTICS:

Female

Postmenopausal, as defined by 1 of the following criteria:

Absence of a menstrual period in the past 12 months

Bilateral oophorectomy

Absence of a menstrual period in the past 6 months with follicle-stimulating hormone (FSH) level > 40 mIU/mL

ECOG performance status 0-1

Life expectancy ≥ 6 months

Willing to provide blood samples during study participation

No history of allergic or other adverse reactions to citalopram hydrobromide or other selective serotonin reuptake inhibitors (SSRIs)

No documented mania or hypomania

PRIOR CONCURRENT THERAPY:

At least 4 weeks since prior and no concurrent antineoplastic chemotherapy

At least 4 weeks since prior and no concurrent androgens, estrogens, or progestational agents

At least 3 months since prior antidepressant use, including Hypericum perforatum (St. John's wort)

Concurrent tamoxifen, raloxifene, or aromatase inhibitors allowed if on a constant dose for ≥ 4 weeks and continuing medication during study period

No other concurrent or planned agents for treating hot flashes (e.g., phenobarbital, megestrol, or clonidine)

Stable dose of vitamin E allowed as long as it was started > 30 days prior to study entry

Concurrent soy allowed

Concurrent gabapentin allowed for reasons other than hot flashes if on a constant dose for ≥ 1 month and continuing during study period