Coenzyme Q10 in Relieving Treatment-Related Fatigue in Women With Breast Cancer
Status: | Completed |
---|---|
Conditions: | Breast Cancer, Cancer, Other Indications |
Therapuetic Areas: | Oncology, Other |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 2/17/2019 |
Start Date: | August 2004 |
End Date: | August 2009 |
A Randomized Double-Blind Placebo-Controlled Study Of Oral Coenzyme Q10 To Relieve Self-Reported Cancer Treatment Related Fatigue In Breast Cancer Patients
RATIONALE: Coenzyme Q10 is a vitamin that may be effective in relieving fatigue and
depression in women who are undergoing chemotherapy for breast cancer.
PURPOSE: This randomized clinical trial is studying how well coenzyme Q10 works in relieving
treatment-related fatigue in women with breast cancer.
depression in women who are undergoing chemotherapy for breast cancer.
PURPOSE: This randomized clinical trial is studying how well coenzyme Q10 works in relieving
treatment-related fatigue in women with breast cancer.
OBJECTIVES:
Primary
- Determine the effect of coenzyme Q_10 on cancer treatment-related fatigue in women with
breast cancer.
Secondary
- Determine the effect of this drug on overall quality of life of these patients.
- Determine the effect of this drug on depression in these patients.
OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients are
stratified according to planned radiotherapy (yes vs no) and type of chemotherapy
(anthracycline vs non-anthracycline). Patients are randomized to 1 of 2 treatment arms.
- Arm I: Beginning on the first day of chemotherapy treatment, patients receive oral
coenzyme Q_10 and oral vitamin E three times daily.
- Arm II: Beginning on the first day of chemotherapy treatment, patients receive oral
vitamin E and an oral placebo three times daily.
Treatment in both arms continues for 24 weeks in the absence of unacceptable toxicity.
Quality of life, fatigue, and depression are assessed at baseline and at 8, 16, and 24 weeks.
PROJECTED ACCRUAL: A total of 101-236 patients will be accrued for this study.
Primary
- Determine the effect of coenzyme Q_10 on cancer treatment-related fatigue in women with
breast cancer.
Secondary
- Determine the effect of this drug on overall quality of life of these patients.
- Determine the effect of this drug on depression in these patients.
OUTLINE: This is a randomized, double-blind, placebo-controlled study. Patients are
stratified according to planned radiotherapy (yes vs no) and type of chemotherapy
(anthracycline vs non-anthracycline). Patients are randomized to 1 of 2 treatment arms.
- Arm I: Beginning on the first day of chemotherapy treatment, patients receive oral
coenzyme Q_10 and oral vitamin E three times daily.
- Arm II: Beginning on the first day of chemotherapy treatment, patients receive oral
vitamin E and an oral placebo three times daily.
Treatment in both arms continues for 24 weeks in the absence of unacceptable toxicity.
Quality of life, fatigue, and depression are assessed at baseline and at 8, 16, and 24 weeks.
PROJECTED ACCRUAL: A total of 101-236 patients will be accrued for this study.
Inclusion Criteria:
- Signed consent
- Hg > 11g/dl; supportive measures (erythropoietin, transfusion, iron therapy) should be
utilized to assist with maintaining Hgb levels
- Total cholesterol > 160mg/dL.
- Female with primary cancer diagnosis (breast)
- Planned adjuvant chemotherapy (neoadjuvant chemotherapy is excluded)
- KPS > 60
- Bilirubin < 1.5 x ULN
- SGOT < 2.5 x ULN
- SGPT < 2.5 x ULN
Exclusion Criteria:
- Recent involuntary weight loss (> 5% of body weight in the past 3 months)
- Statin therapy - current or planned during study. Below is a list of some commonly
used statin drugs.(Note: This is a helpful guide, not a complete list.)
- Atorvastatin (Lipitor)
- Cerivastatin
- Fluvastatin (Lescol)
- Lovastatin (Mevacor, Altocor, Advicor)
- Mevastatin
- Pravastatin (Pravachol)
- Rosuvastatin
- Simvastatin (Zocor)
- Current or planned use of the following medications for fatigue
- Corticosteroids (intermittent use as part of chemotherapy regimen is allowed)
- Amphetamines or other stimulants including methylphenidate (Ritalin)or modafinil
(Provigil)
- Patients diagnosed with uncontrolled hypertension
- Breast cancer patients who are male
- Pregnant women are excluded from participation in this study. A Serum pregnancy test
is required within 1 week of registration if the patient is a woman of childbearing
potential.
- Anticoagulant therapy - current or planned during study (except for maintenance of
catheter patency)
- Patients with uncontrolled thyroid dysfunction
We found this trial at
31
sites
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CCOP - Mount Sinai Medical Center The Mount Sinai Community Clinical Oncology Program (MSCCOP) is...
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1 Medical Center Blvd
Winston-Salem, North Carolina 27103
Winston-Salem, North Carolina 27103
(336) 716-2011
Wake Forest University Comprehensive Cancer Center Our newly expanded Comprehensive Cancer Center is the region’s...
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5301 East Huron River Drive
Ann Arbor, Michigan 48106
Ann Arbor, Michigan 48106
1.877.590.5995
CCOP - Michigan Cancer Research Consortium The Community Clinical Oncology Program (CCOP) is a comprehensive...
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CCOP - Columbus As one of the original 20 CCOPs, the Columbus Community Clinical Oncology...
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Danville Regional Medical Center For more than 120 years, Danville Regional Medical Center has been...
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Pardee Memorial Hospital Pardee Hospital is a not-for-profit community hospital founded in 1953 and is...
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Hilton Head Island, South Carolina 29925
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Martinsville, Virginia 24115
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533 Bolivar Street, Room 420
New Orleans, Louisiana 70112
New Orleans, Louisiana 70112
(504) 568-3435
MBCCOP - LSU Health Sciences Center Established in 1990, the Stanley S. Scott Cancer Center...
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4701 Ogletown-Stanton Road
Newark, Delaware 19713
Newark, Delaware 19713
302-623-4450
CCOP - Christiana Care Health Services Christiana Care's Cancer Research Program is part of a...
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Missouri Baptist Cancer Center The Cancer Center at Missouri Baptist is a member of Heartland...
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CCOP - Cancer Research for the Ozarks Cancer Research for the Ozarks (CRO), also known...
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