Can Flaxseed Prevent Broken Hearts in Women With Breast Cancer Study? (CANFLAX)
Primary Purpose
Cardiotoxicity
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Flax "milk"
Oat fibre "milk"
Sponsored by
About this trial
This is an interventional prevention trial for Cardiotoxicity focused on measuring Cardiotoxicity, Chemotherapy, Flaxseed
Eligibility Criteria
Inclusion Criteria:
- i) ≥18 years old;
- ii) women with newly diagnosed early stage breast cancer (Stage I-IIIA)
- iii) chemotherapy with 5 fluorouracil, epirubicin, and cyclophosphamide (FEC) or adriamycin and cyclophosphamide (AC) for 4 months
Exclusion Criteria:
- i) pre-existing diagnosis of heart failure and/or LVEF<40%
- ii) pre-existing use of anti-hypertensive agents including ACE inhibitors (ACEi) or beta blockers
- iii) planned use of any herbal/antioxidant/fatty acid/nutritional supplements at any time in the duration of the study.
Sites / Locations
- St. Boniface Albrechtsen Research CentreRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
Flax "milk"
Oat fibre "milk"
Arm Description
A total of 30 women will receive flax (FLX) "milk" on a daily basis for a total of 4 months. The FLX "milk" will be composed of BevPur (30 mesh FLX), various gums for texture, vanilla flavoring, several minor ingredients, and water. Each serving contains 15 grams of FLX and 3.75 grams of Omega-3.
A total of 30 women will receive the oat fiber "milk" on a daily basis for a total of 4 months. The oat fibre "milk" will be composed of oat fibre, various gums for texture, vanilla flavoring, several minor ingredients, and water.
Outcomes
Primary Outcome Measures
Left ventricular ejection fraction (LVEF) change
Left ventricular ejection fraction (LVEF %) will be evaluated using transthoracic echocardiography at baseline and 12 month follow-up. A difference in LVEF>10% from baseline will be considered significant.
Secondary Outcome Measures
Full Information
NCT ID
NCT04632407
First Posted
October 21, 2020
Last Updated
November 11, 2020
Sponsor
St. Boniface Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04632407
Brief Title
Can Flaxseed Prevent Broken Hearts in Women With Breast Cancer Study?
Acronym
CANFLAX
Official Title
Can Flaxseed Prevent Broken Hearts in Women With Breast Cancer Study?
Study Type
Interventional
2. Study Status
Record Verification Date
November 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 21, 2020 (Actual)
Primary Completion Date
December 31, 2022 (Anticipated)
Study Completion Date
December 31, 2022 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Boniface Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The main goal of the current research program is to examine the use of nutraceuticals, in particular flaxseed (FLX), in the prevention of Doxorubicin and Trastuzumab (DOX+TRZ) mediated cardiotoxicity in the clinical setting. As Manitoba continues to be one of the top FLX producers in the world, there is an increasing public awareness of the importance of the consumption of this whole grain commodity in the prevention of cancer and cardiovascular disease. In North America, approximately 1 in 8 women will develop breast cancer and will receive treatment with DOX+TRZ. Although women with breast cancer are at risk of developing heart failure due to chemotherapy, FLX has the capacity to prevent this outcome. The purpose of the CANFLAX study is to establish FLX "milk" as an effective method in preventing heart failure in women with breast cancer.
Detailed Description
Cardiovascular toxicity is a potential short and long-term complication of anti-cancer therapy with DOX+TRZ in the breast cancer setting. Although FLX is commonly consumed in up to 30% of women with breast cancer to improve overall disease burden and survival, it is important to study whether this natural dietary agent can also reduce the cardiotoxic side effects of DOX+TRZ in the clinical setting. The investigators hypothesize that the prophylactic consumption of FLX "milk" will prevent adverse cardiovascular remodeling and improve overall functional capacity in women with breast cancer receiving DOX+TRZ therapy. The two specific aims of the CANFLAX study include: Aim 1: FLX "milk" will prevent the development of heart failure in women with early stage breast cancer (EBC) who are treated with DOX+TRZ based chemotherapy; and Aim 2: FLX "milk" will improve cardiac functional capacity in this patient population.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cardiotoxicity
Keywords
Cardiotoxicity, Chemotherapy, Flaxseed
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
The study participants will be randomized to either oat fibre "milk" or flax "milk"
Masking
ParticipantCare ProviderInvestigator
Masking Description
The 2 products (oat fibre "milk" and flax "milk") are assigned a unique ID code.
Allocation
Randomized
Enrollment
60 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Flax "milk"
Arm Type
Experimental
Arm Description
A total of 30 women will receive flax (FLX) "milk" on a daily basis for a total of 4 months. The FLX "milk" will be composed of BevPur (30 mesh FLX), various gums for texture, vanilla flavoring, several minor ingredients, and water. Each serving contains 15 grams of FLX and 3.75 grams of Omega-3.
Arm Title
Oat fibre "milk"
Arm Type
Experimental
Arm Description
A total of 30 women will receive the oat fiber "milk" on a daily basis for a total of 4 months. The oat fibre "milk" will be composed of oat fibre, various gums for texture, vanilla flavoring, several minor ingredients, and water.
Intervention Type
Dietary Supplement
Intervention Name(s)
Flax "milk"
Intervention Description
See above
Intervention Type
Dietary Supplement
Intervention Name(s)
Oat fibre "milk"
Intervention Description
See above
Primary Outcome Measure Information:
Title
Left ventricular ejection fraction (LVEF) change
Description
Left ventricular ejection fraction (LVEF %) will be evaluated using transthoracic echocardiography at baseline and 12 month follow-up. A difference in LVEF>10% from baseline will be considered significant.
Time Frame
1 year
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
i) ≥18 years old;
ii) women with newly diagnosed early stage breast cancer (Stage I-IIIA)
iii) chemotherapy with 5 fluorouracil, epirubicin, and cyclophosphamide (FEC) or adriamycin and cyclophosphamide (AC) for 4 months
Exclusion Criteria:
i) pre-existing diagnosis of heart failure and/or LVEF<40%
ii) pre-existing use of anti-hypertensive agents including ACE inhibitors (ACEi) or beta blockers
iii) planned use of any herbal/antioxidant/fatty acid/nutritional supplements at any time in the duration of the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Davinder S Jassal, MD
Phone
2042372023
Email
djassal@sbgh.mb.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Davinder S Jassal, MD
Organizational Affiliation
University of Manitoba
Official's Role
Principal Investigator
Facility Information:
Facility Name
St. Boniface Albrechtsen Research Centre
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R2E1J7
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Davinder S Jassal, MD
Phone
2042372023
Email
djassal@sbgh.mb.ca
12. IPD Sharing Statement
Plan to Share IPD
No
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