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Solifenacin Compared to Clonidine for Reducing Hot Flashes Among Breast Cancer Patients

Phase 2
Recruiting
Conditions
Breast Cancer
Hot Flashes
Interventions
Registration Number
NCT01530373
Lead Sponsor
University of Arkansas
Brief Summary

Hot flashes present a considerable problem for many breast cancer patients; these symptoms may be intensified by hormonal therapies, such as aromatase inhibitors or tamoxifen. This study examines the value of solifenacin (a muscarinic acetylcholine receptor antagonist) in reducing hot flashes, compared with clonidine (a medication often used for treating hot flashes).

Detailed Description

There has been considerable interest in developing new treatment strategies for managing hot flashes among women with breast cancer, in view of the limitations associated with currently available treatments. This randomized study evaluates the safety and efficacy of 3 weeks of solifenacin compared to 3 weeks of clonidine, for women receiving adjuvant hormonal therapy (aromatase inhibitors or tamoxifen) for breast cancer.

Recruitment & Eligibility

Status
RECRUITING
Sex
Female
Target Recruitment
110
Inclusion Criteria
  • Women with a history of invasive breast cancer or DCIS
  • Currently taking aromatase inhibitors or tamoxifen
  • Not receiving hormone replacement therapy for minimum of one month
  • Age 18 years or older
  • Self-reported hot flashes at least fourteen times per week
  • Self-reported hot flashes for at least one month
  • If receiving non-tricyclic antidepressants (venlafaxine, paroxetine, citalopram, sertraline, etc.) or gabapentin, no change in regimen in past 4 weeks.
Exclusion Criteria
  • Receiving any other treatment for hot flashes within the past month, including estrogens, progestins, androgens, or gabapentin.
  • Current use of clonidine or solifenacin. (If patients have been off of these for one month, then they are eligible)
  • History of severe renal or moderate or severe hepatic impairment, as indicated by physical exam and medical record
  • Concurrent or planned chemotherapy or radiotherapy (within next 3 months)
  • Currently receiving tricyclic antidepressants, monoamine oxidase inhibitors, barbiturates, pimozide.
  • Currently using CYP3A4 inducers (i.e., aminoglutethimide, carbamazepine, dexamethasone, efavirenz, ethosuximide, griseofulvin, modafinil, nafcillin, nevirapine, oxcarbazepine, phenobarbital, phenylbutazone, phenytoin, primidone, rifabutin, rifampin, rifapentine, St. John's Wort, sulfadimidine, sulfinpyrazone, troglitazone) or potent CYP3A4 inhibitors (i.e., chloramphenicol, clarithromycin, erythromycin, imatinib mesylate, indinavir sulfate, itraconazole, ketoconazole, nefazoldone, nelfinavir mesylate, ritonavir, telithromycin, troleandomycin).
  • Uncontrolled or poorly controlled narrow-angle glaucoma, urinary retention, gastric retention (evaluated from history & physical exam and medical record)
  • Hypotension or uncontrolled hypertension (160/95 > BP < 100/60)
  • Severe coronary insufficiency, conduction disturbances, recent myocardial infarction (within past 3 months), cerebrovascular disease, syncope (evaluated from history & physical and medical record)
  • History of allergy or adverse reactions to clonidine or solifenacin
  • ECOG status > 2 (in bed more than 50% of day)

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
solifenacinsolifenacinoral solifenacin 5.0 mg daily for 3 weeks
clonidineClonidineoral clonidine 0.1 mg daily for 3 weeks
Primary Outcome Measures
NameTimeMethod
Efficacy: hot flash composite and frequency scores (daily diary)from baseline to end of treatment (3 weeks)

to evaluate changes in hot flash composite and frequency scores for women receiving 3 weeks of oral solifenacin compared to those receiving 3 weeks of oral clonidine

Safety: number of clinician-rated adverse eventsfrom consent until end of study (approximately 9 weeks)

to evaluate changes in number of adverse events for women receiving 3 weeks of oral solifenacin compared to those receiving 3 weeks of oral clonidine

Secondary Outcome Measures
NameTimeMethod
sleep (Insomnia Severity Index)from baseline to end of treatment (3 weeks)

To evaluate changes in sleep

daily functioning (Hot Flash-Related Daily Interference score)from baseline to end of treatment (3 weeks)

to evaluate changes in daily functioning (Hot Flash-Related Daily Interference Score) for women receiving 3 weeks of oral solifenacin compared to those receiving 3 weeks of oral clonidine

quality of life (Illness Cognition Questionnaire, SF-12)from baseline to end of treatment (3 weeks)

to evaluate changes in health-related quality of life. (Additional analyses will be observational, exploring associations between quality of life and meaning-making.)

Trial Locations

Locations (1)

Winthrop P. Rockefeller Cancer Institute, University of Arkansas for Medical Sciences

🇺🇸

Little Rock, Arkansas, United States

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