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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
Texas Tech University Health Sciences Center, El Paso
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

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

    First Posted
    February 10, 2017
    Last Updated
    January 24, 2018
    Sponsor
    Texas Tech University Health Sciences Center, El Paso
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    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

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    Vitamin B12 for Aromatase Inhibitors Musculoskeletal Symptoms

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