CANFLAX: Can Flaxseed Prevent Broken Hearts in Women With Breast Cancer Study?

Sponsor
St. Boniface Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT04632407
Collaborator
(none)
60
1
2
26.3
2.3

Study Details

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.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Flax "milk"
  • Dietary Supplement: Oat fibre "milk"
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
The study participants will be randomized to either oat fibre "milk" or flax "milk"The study participants will be randomized to either oat fibre "milk" or flax "milk"
Masking:
Triple (Participant, Care Provider, Investigator)
Masking Description:
The 2 products (oat fibre "milk" and flax "milk") are assigned a unique ID code.
Primary Purpose:
Prevention
Official Title:
Can Flaxseed Prevent Broken Hearts in Women With Breast Cancer Study?
Actual Study Start Date :
Oct 21, 2020
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Experimental: Flax "milk"

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.

Dietary Supplement: Flax "milk"
See above

Experimental: Oat fibre "milk"

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.

Dietary Supplement: Oat fibre "milk"
See above

Outcome Measures

Primary Outcome Measures

  1. Left ventricular ejection fraction (LVEF) change [1 year]

    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.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
    1. ≥18 years old;
    1. women with newly diagnosed early stage breast cancer (Stage I-IIIA)
    1. chemotherapy with 5 fluorouracil, epirubicin, and cyclophosphamide (FEC) or adriamycin and cyclophosphamide (AC) for 4 months
Exclusion Criteria:
    1. pre-existing diagnosis of heart failure and/or LVEF<40%
    1. pre-existing use of anti-hypertensive agents including ACE inhibitors (ACEi) or beta blockers
    1. planned use of any herbal/antioxidant/fatty acid/nutritional supplements at any time in the duration of the study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 St. Boniface Albrechtsen Research Centre Winnipeg Manitoba Canada R2E1J7

Sponsors and Collaborators

  • St. Boniface Hospital

Investigators

  • Principal Investigator: Davinder S Jassal, MD, University of Manitoba

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Dr. Davinder S. Jassal, Professor of Medicine, St. Boniface Hospital
ClinicalTrials.gov Identifier:
NCT04632407
Other Study ID Numbers:
  • CT/2019/CANFLAX
First Posted:
Nov 17, 2020
Last Update Posted:
Nov 17, 2020
Last Verified:
Nov 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Dr. Davinder S. Jassal, Professor of Medicine, St. Boniface Hospital
Additional relevant MeSH terms:

Study Results

No Results Posted as of Nov 17, 2020