A Randomized Double-blind, Placebo Controlled, Multi-center Study to Evaluate the Safety, Tolerability and Potential Effects of the Dietary Supplement Violet™ Molecular Iodine (I2) on Breast Health in Women With Cyclic Breast Discomfort and Tenderness

Not Applicable

Completed

• Conditions: Fibrocystic Breast Condition (FBC)
• Interventions: Dietary Supplement: Violet™ Molecular Iodine (I2); Other: Placebo

• Registration Number: NCT02676336
• Lead Sponsor: BioPharmX, Inc.

Brief Summary

This is a randomized, double-blind, placebo controlled, multi-center study to evaluate the safety, tolerability and potential effects of dietary supplement Violet™ Iodine on breast health in women with cyclic breast discomfort and tenderness to eliminate the evaluation of effectiveness.

Detailed Description

Not available

Study Timeline

• Study Start: 2016-02
• Study First Submitted: 2016-02-03
• Study First Submitted QC: 2016-02-05
• Study First Posted: 2016-02-08
• Primary Completion: 2018-01-31
• Study Completion: 2018-01-31
• Status Verified: 2018-07
• Last Update Submitted: 2018-07-09
• Last Update Posted: 2018-07-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 31

Inclusion Criteria

• Healthy premenopausal females ≥ 18 years of age
• BMI 20.0 - 29.9 kg/m2 (± 1 kg/m2)
• Females of childbearing potential must agree to use a reliable and consistent method of birth control in the Investigator's opinion, excluding depot contraceptives and Explanon, and have a negative urine pregnancy test result. Hormonal contraceptives such as oral contraceptives, birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing) are all acceptable as long as the subject is on a stable dose and agrees not to change during the study period
• No apparent health conditions that in the investigator's opinion would interfere with study participation, compliance or interpretation of endpoints or would not be in the best interest of the subject
• Moderate to severe cyclic breast discomfort of at least 4 days per month (discomfort ≥4 on a 0-10 scale)
• No known medical or psychological condition that in the investigator's opinion could interfere with study participation
• Agrees to comply with all study related procedures and visits including access to a smartphone (Android or iOS) and ability to enter daily diary information via a smart phone app
• Capable of reading and understanding study related materials (in English or French) and has given voluntary, written, informed consent to participate in the study

Exclusion Criteria

• Women who are pregnant, breast feeding, or planning to become pregnant during the course of the trial
• Perimenopausal or irregular menstrual cycles
• Women who have had an oophorectomy
• Known thyroid condition or currently taking any thyroid medications
• Prior bariatric surgery or other interventions or medications that might affect gastric pH
• Use of iodine supplementation, Tamoxifen, Lupron, or Danazol, in the last 6 months
• Clinically significant abnormal laboratory results at Screening
• Breast implant surgeries that have not fully healed or have ongoing problems associated with the implant (i.e. seroma, infection etc.)
• Planned elective surgeries to occur during participation in the study
• Known allergy or sensitivity to study product ingredients (e.g. Iodine)
• History of alcohol or drug abuse within the past year
• Use of medicinal marijuana within the past year
• Participation in a clinical research trial within 30 days prior to randomization or plans to participate in any other study during the next 11 months
• Individuals who are cognitively impaired and/or who are unable to give informed consent
• Any other condition which in the Investigator's opinion may adversely affect the subject's ability to complete the study or its measures, may confound interpretation of study outcome measures (such as another condition) or which may pose significant risk to the subject

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Violet™ Iodine	Violet™ Molecular Iodine (I2)	3mg molecular iodine (I2) daily
Placebo	Placebo	3mg placebo daily
Cross-over	Violet™ Molecular Iodine (I2)	Subjects on placebo will be offered 3 months of active post-treatment

Primary Outcome Measures

Name	Time	Method
Change in self assessed cyclic breast discomfort	After 6 months of active treatment with molecular iodine (I2) compared to placebo

Trial Locations

Locations (1)

KGK Synergize; 🇨🇦 London, Ontario, Canada