Vitamin B12 for Aromatase Inhibitors Musculoskeletal Symptoms
Primary Purpose
Relief of Joint Pain
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Vitamin B12
Sponsored by
About this trial
This is an interventional treatment trial for Relief of Joint Pain focused on measuring Aromatase Inhibitor, Breast Cancer, Arthralgia, Musculoskeletal symptoms, Joint pain
Eligibility Criteria
Inclusion Criteria:
- Sign informed consent and Pain level > 4 in the BPI scale,
- Stage I-III
Exclusion Criteria:
- <18 yrs
- Stage IV
- BPI Score <4
- Zubrod score >2
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Arm I
Arm Description
Oral Vitamin B12
Outcomes
Primary Outcome Measures
Percentage Change in Average Joint Pain in Women With Aromatase Inhibitor-associated Musculoskeletal Symptoms (AIMSS) Compared to Baseline as Measured by the Brief Pain Inventory Short Form (BPI-SF).
The Brief Pain Inventory - Short Form (BPI- SF) average pain score used. This item has a scale of 0 to 10 with 0 indicating "No pain" and 10 indicating "Pain as bad as you can imagine" We expect at least 20% improvement in BPI-SF pain scores. Participants were asked to rate worst pain an average pain within the last 24 hours.
Secondary Outcome Measures
Percentage Change in Worst Pain at the End of Treatment .
Analysis of the data collected at baseline and at the end of treatment in the BPI-SF questionnaire. The Brief Pain Inventory - Short Form (BPI- SF) worst pain score used. This item has a scale of 0 to 10 with 0 indicating "No pain" and 10 indicating "Pain as bad as you can imagine". Participants were asked to rate worst pain an average pain within the last 24 hours.
Percentage Change in Functional Quality of Life as Measured by the Functional Assessment of Cancer Therapy-Endocrine Scale (FACT-ES)
All of the items in this questionnaire have a 5 scale rating, from not at all (0) to very much (4). Outcomes were measured pre and post treatment. Version 4 of the FACT-ES contains 3 subscales with seven questions: Physical Well-Being (PWB) (score range 0-28), Functional Well-Being (FWB) (score range 0-28), and Social and Well-Being (SWB) (score range 0-28); Emotional Well-Being (EWB) (score range 0-24) with six questions, and the Endocrine Symptom Subscale (ESS) (score range 0-76) containing 19 questions. For all subscale a higher score represents better quality of life.
Percentage Change of Serum Levels of Vitamin B12, C-reactive Protein (CRP), Homoscyteine (HCys) and Methylmalonic Acid (MMA).
Inflammatory markers were measured pre and post treatment.
Full Information
NCT ID
NCT03069313
First Posted
February 10, 2017
Last Updated
January 24, 2018
Sponsor
Texas Tech University Health Sciences Center, El Paso
1. Study Identification
Unique Protocol Identification Number
NCT03069313
Brief Title
Vitamin B12 for Aromatase Inhibitors Musculoskeletal Symptoms
Official Title
A Single Arm Phase II Study of Oral Vitamin B12 for the Treatment of Aromatase Inhibitors (AI) Associated Musculoskeletal Symptoms in Women With Early Stage Breast Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
October 19, 2015 (Actual)
Primary Completion Date
October 27, 2016 (Actual)
Study Completion Date
October 27, 2016 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Texas Tech University Health Sciences Center, El Paso
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
Significant Aromatase Inhibitor-associated toxicity, affects as many as 50% of patients with breast cancer leading to early discontinuation of this life-saving cancer treatment. No effective pharmacologic therapy has yet been identified for management of these symptoms, as many patients do not experience relief of symptoms with analgesic therapy. Vitamin B12, whether as injection or oral forms, has been used as a naturopathic product to provide relief for joint pain caused by arthritis. This effect has not been studied in the setting of Aromatase Inhibitor-Associated Musculoskeletal Symptoms (AIMSS).
Detailed Description
Primary Objectives:
a. To assess whether daily oral Vitamin B12 decreases average joint pain in women with aromatase inhibitor-associated musculoskeletal symptoms (AIMSS), as measured at baseline, 6 weeks and at 12 weeks by the modified Brief Pain Inventory Short Form (BPI-SF).
Secondary Objectives:
To investigate whether daily vitamin B12 improves functional quality of life as measured by the Functional Assessment of Cancer Therapy-Endocrine Scale (FACT-ES);
To explore the impact of treatment on serum inflammatory cytokine levels (C Reactive Protein) with 12 weeks of treatment between baseline and 12 weeks.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Relief of Joint Pain
Keywords
Aromatase Inhibitor, Breast Cancer, Arthralgia, Musculoskeletal symptoms, Joint pain
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Vitamin B12 is to be taken sublingually on a daily basis for 90 days
Masking
None (Open Label)
Allocation
N/A
Enrollment
41 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Arm I
Arm Type
Experimental
Arm Description
Oral Vitamin B12
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin B12
Intervention Description
Vitamin B12 2500 micrograms sublingually per day over the course of 90 days (+/- 10 days)
Primary Outcome Measure Information:
Title
Percentage Change in Average Joint Pain in Women With Aromatase Inhibitor-associated Musculoskeletal Symptoms (AIMSS) Compared to Baseline as Measured by the Brief Pain Inventory Short Form (BPI-SF).
Description
The Brief Pain Inventory - Short Form (BPI- SF) average pain score used. This item has a scale of 0 to 10 with 0 indicating "No pain" and 10 indicating "Pain as bad as you can imagine" We expect at least 20% improvement in BPI-SF pain scores. Participants were asked to rate worst pain an average pain within the last 24 hours.
Time Frame
Baseline and 90 days (+/- 10 days)
Secondary Outcome Measure Information:
Title
Percentage Change in Worst Pain at the End of Treatment .
Description
Analysis of the data collected at baseline and at the end of treatment in the BPI-SF questionnaire. The Brief Pain Inventory - Short Form (BPI- SF) worst pain score used. This item has a scale of 0 to 10 with 0 indicating "No pain" and 10 indicating "Pain as bad as you can imagine". Participants were asked to rate worst pain an average pain within the last 24 hours.
Time Frame
Baseline and 90 days (+/- 10 days)
Title
Percentage Change in Functional Quality of Life as Measured by the Functional Assessment of Cancer Therapy-Endocrine Scale (FACT-ES)
Description
All of the items in this questionnaire have a 5 scale rating, from not at all (0) to very much (4). Outcomes were measured pre and post treatment. Version 4 of the FACT-ES contains 3 subscales with seven questions: Physical Well-Being (PWB) (score range 0-28), Functional Well-Being (FWB) (score range 0-28), and Social and Well-Being (SWB) (score range 0-28); Emotional Well-Being (EWB) (score range 0-24) with six questions, and the Endocrine Symptom Subscale (ESS) (score range 0-76) containing 19 questions. For all subscale a higher score represents better quality of life.
Time Frame
Baseline and 90 days (+/- 10 days)
Title
Percentage Change of Serum Levels of Vitamin B12, C-reactive Protein (CRP), Homoscyteine (HCys) and Methylmalonic Acid (MMA).
Description
Inflammatory markers were measured pre and post treatment.
Time Frame
Baseline and at 90 days (+/- 10 days)
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Breast cancer patients
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Sign informed consent and Pain level > 4 in the BPI scale,
Stage I-III
Exclusion Criteria:
<18 yrs
Stage IV
BPI Score <4
Zubrod score >2
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zeina Nahleh, MD
Organizational Affiliation
Texas Tech University HSC El Paso
Official's Role
Principal Investigator
12. IPD Sharing Statement
Plan to Share IPD
Undecided
Learn more about this trial
Vitamin B12 for Aromatase Inhibitors Musculoskeletal Symptoms
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