Venlafaxine With or Without Zolpidem in Treating Hot Flashes and Associated Sleep Disorders in Women With Breast Cancer OR at High Risk for Developing Breast Cancer
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00084669|
Recruitment Status : Completed
First Posted : June 11, 2004
Last Update Posted : April 28, 2010
RATIONALE: Venlafaxine may be effective in relieving hot flashes caused by hormone therapy. Giving venlafaxine with zolpidem (a sleeping pill) may improve sleep and quality of life in women who are receiving hormone therapy for treatment or prevention of breast cancer.
PURPOSE: This randomized clinical trial is studying giving venlafaxine together with zolpidem to see how well it works compared to venlafaxine alone in relieving hot flashes and associated sleep disorders in women who are receiving hormone therapy to treat or prevent breast cancer.
|Condition or disease||Intervention/treatment|
|Breast Cancer Hot Flashes Sleep Disorders||Drug: venlafaxine Drug: zolpidem tartrate Procedure: management of therapy complications|
- Compare the effect of venlafaxine or another serotonin-reuptake inhibitor with vs without zolpidem, in terms of sleep continuity, in women with breast cancer or at high risk for developing breast cancer who experience hot flushes and associated sleep disorders.
- Compare quality of life in patients treated with these regimens.
OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients are stratified by concurrent use of serotonin-reuptake inhibitors (SRI).
Stratum 1 (no concurrent SRI): Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive oral venlafaxine once daily and oral zolpidem once daily for 5 weeks*.
- Arm II: Patients receive oral venlafaxine once daily and oral placebo once daily for 5 weeks*.
Stratum 2 (concurrently on SRI): Patients are randomized to 1 of 2 treatment arms.
- Arm I: Patients receive oral zolpidem once daily for 5 weeks*.
- Arm II: Patients receive oral placebo once daily for 5 weeks*. NOTE: *After 5 weeks of study treatment, patients in stratum 1 may taper or continue venlafaxine over 2 weeks (for a total duration of venlafaxine use of 7 weeks); patients in arm I of both strata may taper or continue zolpidem over 1 week (for a total duration of zolpidem use of 6 weeks); continuation or tapering of drugs in both arms occurs in an open-label fashion off study.
In both strata, treatment continues in the absence of unacceptable toxicity.
In both strata, hot flushes, sleep continuity, sleep quality, and quality of life are assessed at baseline and at weeks 1, 3, and 6.
PROJECTED ACCRUAL: A total of 119 patients will be accrued for this study within 20 months.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||119 participants|
|Primary Purpose:||Supportive Care|
|Official Title:||Targeting Insomnia to Enhance Hot Flush Treatment in Women Receiving Therapy for Breast Cancer or Breast Cancer Risk-Reduction|
|Study Start Date :||May 2004|
|Primary Completion Date :||October 2007|
|Study Completion Date :||March 2010|
- Sleep improvement by biologic data and actigraphy data at the end of study treatment
- Quality of life by BDI, QOLI, PSI, NCCTG symptom diary, PSQI, MOS SF-36 at the end of study treatment
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00084669
|United States, Massachusetts|
|Massachusetts General Hospital|
|Boston, Massachusetts, United States, 02114|
|Dana-Farber/Harvard Cancer Center at Dana Farber Cancer Institute|
|Boston, Massachusetts, United States, 02115-6084|
|Study Chair:||Hadine Joffe, MD, MSC||Massachusetts General Hospital|