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CompletedNCT00275704Updated Jun 10, 2011

Flaxseed for the Treatment of Hot Flashes

A Phase 2 interventional study of Flaxseed in Hot Flashes, sponsored by Mayo Clinic. Completed at 1 site in United States. Open to female participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2011-06-10.

Sponsored by Mayo Clinic · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
30
Allocation
Non-randomized
Ages
18 Years and older
Sex
Female
01

Study summary

Flaxseed, a phytoestrogen, is a natural food supplement rich in plant ligands, which have a very weak estrogen effect. In this study, flaxseed is being evaluated in regard to its capacity to safely and effectively treat hot flashes. Specifically, this study seeks to determine if flaxseed will lower the number and severity of hot flashes and if women experience any side effects from taking flaxseed for this purpose.

02

Conditions studied

  • Hot Flashes

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03

In context

Hot Flashes

285 studies on the registry are indexed under Hot Flashes; 50 are open to participants now.

This study's enrollment of 30 is below the median of 90 across 255 interventional studies indexed under Hot Flashes.

Browse Hot Flashes studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,218 studies on the registry; 670 are open to participants now.

Of its 445 completed or terminated interventional studies of FDA-regulated products, 313 (70%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age greater than or equal to 18 years
  • Women with a history of breast cancer (currently without malignant disease) or women who have no history of breast cancer but who wish to avoid estrogen due to a perceived increased risk of breast cancer.
  • Bothersome hot flashes (defined by occurenece of greater than or equal to 14 times per week and of sufficient severity to make the patient desire therapeutic intervention).
  • Presence of hot flashes for greater than or equal to 1 month prior to study entry.
  • Life expectancy greater than or equal to 6 months.
  • ECOG Performance Status (PS) 0 or 1 (see Appendix VIII)

Exclusion criteria

Exclusionary Criteria/Contraindications

  • Any of the following current (less than or equal to 4 weeks) or planned therapies (tamoxifen, raloxifene, or aromatase inhibitors are allowed, but patient must have been on a constant dose for greater than or equal to 4 weeks and must not be expected to stop the medication during the study period): antineoplastic chemotherapy, androgens, estrogens, progestational agents, other herbal supplements, including soy (herbal teas from a grocery store are allowed), warfarin (1 mg of daily warfarin is allowed for central line patency)
  • History of allergic or other adverse reaction to flaxseed, wheat, nuts, lactose, and/or certain spices
  • Current or planned use of other agents for treating hot flashes (except stable dose of vitamine E or antidepressants are allowed as long as they wre started >30 days prior to study initiation and are to be continued through the study period).
  • Diabetes (as flaxseed can lower blood glucose levels and might have additive effects when used with antidiabetic drugs).
  • Diagnosis of/problems with chronic diarrhea or history of bowel obstruction or esophageal stricture.
  • Any of the following: pregnant women, nursing women, women of childbearing potential who are unwilling to employ adequate contraception
  • Current use of anticoagulants including aspirin, clopidogrel (Plavix), ticlopidine (Ticlic), and coumadin (1 mg of dialy coumadin is allowed for central line patency).
  • Diagnosis of/problems with von Willebrand's disease or other bleeding disorders.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
30 participants

Interventions

  • DrugFlaxseed
06

What researchers measure

Primary outcomes

  1. Determine if flaxseed will lower the number and severity of hot flashes

  2. Determine if there are any side effects from taking flaxseed for hot flashes

  3. Evaluate the impact of flaxseed on hot flash scores in women with a history of breast cancer or women who do not wish to take estrogen therapy for fear of increased risk of breast cancer.

  4. Evaluate the toxicity of flaxseed in this study population.

  5. Evaluate the effect of flaxseed on quality-of-life measures.

07

Study locations

1 site
  • Mayo Clinic
    Rochester, Minnesota 55905, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 10, 2011, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00275704
Lead sponsor
Mayo Clinic
Collaborators
Susan G. Komen Breast Cancer Foundation
First posted
Jan 12, 2006
Start date
May 2005
Primary completion
Jun 2006
Last update
Jun 10, 2011

Study contacts

Sandhya Pruthi, M.D.
principal investigator · Mayo Clinic
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2011. You cannot join it, but the record below documents what was studied.

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