- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01965522
Anti-proliferative Effects of Vitamin D and Melatonin in Breast Cancer (MELO-D)
June 14, 2017 updated by: Punam Rana, Juravinski Cancer Center
Investigators plan to carry out a study to investigate two different pills, Vitamin D and melatonin, and whether they can reduce the spread of cancer cells in the tumors of women with breast cancer.
These pills are inexpensive and have very few side effects.
A large number of studies using cell cultures and animals have shown that both vitamin D and melatonin can help destroy breast cancer cells.
However thoughtful and well-designed studies are necessary on humans to see if they can decrease the spread of breast cancer, and possibly even prevent breast cancer.
The proposed study aims to understand the anti-cancer activity of vitamin D and melatonin.
This knowledge will assist in creating efficient cancer prevention strategies for Canadians.
This study will include women with breast cancer who are being planned for surgery, and will assess whether treatment with vitamin D (dose of 2000 IU per day) in a group of 36 women, or melatonin (dose of 20mg per day) in another group of 36 women, or both pills together in yet another group of 36 women, reduces the spread of cancer cells when compared to a fourth group of 36 women who are treated with sugar pills.
To do this we will measure a substance in the blood called Ki67, which provides information about the spread of cancer.
Investigators will compare the Ki67 levels in the 4 groups, and all women will receive identical appearing pills so they will not know which treatment they received.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
100
Phase
- Phase 2
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ontario
-
Hamilton, Ontario, Canada, L8N 1Y3
- St Joseph's Healthcare Hamilton
-
Hamilton, Ontario, Canada, L8V 1C3
- Juravinski Cancer Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Woman with histologically confirmed invasive breast cancer (ductal, lobular, or mixed)
- Planned to undergo definitive surgery, either lumpectomy or mastectomy in 3 or more weeks
Exclusion Criteria:
- Less than 18 years of age
- Stage IIIB or IV disease
- Inoperable locally advanced or metastatic breast cancer
- Neoadjuvant chemotherapy is intended
- Currently taking vitamin D supplements
- Currently taking melatonin supplements
- Previously taking vitamin D or melatonin supplements within the last 3 months
- Currently taking a multivitamin and not willing to discontinue for the duration of the study
- Hyperparathyroid disease or other calcium disturbance in the past five years
- Active renal stones in the last six months
- Renal failure (creatinine > 190 mmol/L)
- Hypercalcemia (serum calcium > 2.6 mmol/L)
- Known pregnancy
- Participation in another clinical trial where the patient receives any other investigational product
- Unwilling or unable to provide informed consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Quadruple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Melatonin and Vitamin D
|
Melatonin 20mg taken orally once daily.
This is in the form of one capsule which contains two pills of melatonin, 10 mg each.
Vitamin D 2000 IU taken orally once daily.
This is in the form of one capsule which contains two pills of vitamin D, 1000 IU each.
|
|
Experimental: Placebo and Vitamin D
|
Vitamin D 2000 IU taken orally once daily.
This is in the form of one capsule which contains two pills of vitamin D, 1000 IU each.
Overencapsulated placebo capsule which contains an inert substance.
The capsule appears identical to the capsule which contains melatonin tablets.
|
|
Experimental: Melatonin and Placebo
|
Melatonin 20mg taken orally once daily.
This is in the form of one capsule which contains two pills of melatonin, 10 mg each.
Overencapsulated placebo capsule which contains an inert substance.
The capsule appears identical to the capsule which contains vitamin D tablets.
|
|
Placebo Comparator: Placebo and Placebo
|
Overencapsulated placebo capsule which contains an inert substance.
The capsule appears identical to the capsule which contains melatonin tablets.
Overencapsulated placebo capsule which contains an inert substance.
The capsule appears identical to the capsule which contains vitamin D tablets.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Ki67
Time Frame: From time of initial biopsy to the final surgery, which is on average 4 weeks
|
The primary outcome is the difference in proliferation rate of Ki67 in the tumour (expressed as the percentage of tumour cells expressing Ki67).
Ki67 will be measured on the original core biopsy (pre-treatment) and on the lumpectomy/mastectomy specimen (post-treatment).
|
From time of initial biopsy to the final surgery, which is on average 4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
microRNA
Time Frame: At the time of surgery compared to time of biopsy, which is on average 4 weeks
|
Change in serum profile of microRNA at the time of surgery (lumpectomy or mastectomy, post-treatment) will be compared to the time of initial biopsy (pre-treatment).
|
At the time of surgery compared to time of biopsy, which is on average 4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
October 1, 2013
Primary Completion (Actual)
August 1, 2016
Study Completion (Actual)
May 1, 2017
Study Registration Dates
First Submitted
October 11, 2013
First Submitted That Met QC Criteria
October 15, 2013
First Posted (Estimate)
October 18, 2013
Study Record Updates
Last Update Posted (Actual)
June 16, 2017
Last Update Submitted That Met QC Criteria
June 14, 2017
Last Verified
June 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
- Skin Diseases
- Neoplasms
- Neoplasms by Site
- Breast Diseases
- Breast Neoplasms
- Physiological Effects of Drugs
- Molecular Mechanisms of Pharmacological Action
- Central Nervous System Depressants
- Protective Agents
- Micronutrients
- Bone Density Conservation Agents
- Calcium-Regulating Hormones and Agents
- Antioxidants
- Vitamin D
- Cholecalciferol
- Melatonin
- Vitamins
- Ergocalciferols
Other Study ID Numbers
- MELO-D
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
Clinical Trials on Early Stage Breast Cancer
-
Fudan UniversityNot yet recruitingBreast Cancer Early Stage Breast Cancer (Stage 1-3)China
-
M.D. Anderson Cancer CenterActive, not recruitingAnatomic Stage I Breast Cancer AJCC v8 | Anatomic Stage II Breast Cancer AJCC v8 | Early Stage Triple-Negative Breast Carcinoma | Early Stage HER2-Positive Breast CarcinomaUnited States
-
Hoffmann-La RocheRecruitingEarly-stage HER2+ Breast CancerSerbia
-
Cancer Institute and Hospital, Chinese Academy...Not yet recruitingBreast Cancer Early Stage Breast Cancer (Stage 1-3) | HR Positive/HER2 Low Breast CancerChina
-
Rutgers, The State University of New JerseyRecruitingHER2-positive Early-stage Breast CancerUnited States
-
Peking University People's HospitalRecruitingHER2-negative Breast Cancer | Breast Cancer Early Stage Breast Cancer (Stage 1-3) | Hormone Receptor-Positive Breast Cancer | Early-Stage Breast Cancer | ctDNA Monitoring | High-risk Breast CancerChina
-
The Netherlands Cancer InstituteBOOG Study Center; Stichting Treatmeds; Zorgevaluatie en Gepast Gebruik (ZE&GG); Integraal Kankercentrum Nederland (IKNL)Not yet recruitingBreast Cancer Stage II | Breast Cancer Stage III | Triple -Negative Breast Cancer | Early Stage Triple-Negative Breast Carcinoma | Triple Negative Breast Cancer (TNBC), Early Setting
-
M.D. Anderson Cancer CenterRecruitingAerobic Exercise | Early Stage Triple Negative Breast CancerUnited States
-
Dana-Farber Cancer InstituteCompletedEarly Stage Breast Cancer | Breast Cancer Stage I | Breast Cancer Stage IIUnited States
-
St. Antonius HospitalRijnstate Hospital; Amphia Hospital; Antoni van Leeuwenhoek HospitalNot yet recruitingBreast Cancer Stage I | Breast Cancer Early Stage Breast Cancer (Stage 1-3)Netherlands
Clinical Trials on Melatonin
-
Ain Shams UniversityCompleted
-
Duquesne UniversityCompleted
-
Suez Canal UniversityActive, not recruiting
-
Suez Canal UniversityActive, not recruiting
-
Bangladesh Medical UniversityEnrolling by invitationParkinson DiseaseBangladesh
-
Peking Union Medical College HospitalCompleted
-
Benha UniversityRecruitingPain Management | Cesarean Section Pain | Pain After SurgeryEgypt
-
Liaquat College of Medicine and DentistryCompletedPeriodontal Disease | MelatoninPakistan
-
Chinese PLA General HospitalUnknown
-
Assaf-Harofeh Medical CenterNeurim Pharmaceuticals Ltd.UnknownMild Cognitive Impairment (MCI)Israel