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Evaluation of the Efficiacy of Mecobalamine in the Treatment of Long-term Pain in Women Diagnosed With Fibromyalgia

Primary Purpose

Fibromyalgia

Status
Recruiting
Phase
Phase 1
Locations
Sweden
Study Type
Interventional
Intervention
Mecobalamin 5 MG
Placebo Comparator : NaCl 9 mg/ml
Sponsored by
Linnaeus University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fibromyalgia focused on measuring Fibromyalgia,, Chronic pain,, Mekobalamin,, Randomized Controlled Trial, VitaminB12

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Women aged 20-70 years
  • Swedish-speaking
  • Diagnosis of fibromyalgia
  • Safe method of contraception
  • Cobalamin / p (vitamin B12) should be >250 pmol/L < 800 pmol/L
  • Given consent to participate.

Exclusion Criteria:

  • Previous treatment with B12
  • Known hypersensitivity to the active substance Mecobalamin or an additive
  • Vegan as veganism can lead to B12 deficiency
  • Neuroleptics
  • Known heart, kidney or liver disease
  • Reynaud's phenomenon (white fingers)
  • Known neuropathy (impaired sensation)
  • Breastfeeding
  • Pregnancy or plan pregnancy

Sites / Locations

  • Linnaeus UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Mecobalamine 5 mg/ml

NaCl 9mg/ml

Arm Description

The active substance of vitamin B12 given in the study is Mecobalamin 5mg / ml 2 ml ie 10 mg and is given intramuscularly.

Placebo substance given in the study is Sodium Chloride (NaCL) 9 mg / ml 2 ml, isotonic solution for parenteral use (Baxter) given intramuscularly.

Outcomes

Primary Outcome Measures

Tolerance time
Primary outcome is tolerance time, maximized to Three minutes, tested using the Cold Pressure test

Secondary Outcome Measures

Pain experience measured by a pressure algometry test
Pain experience measured by a pressure algometry test performed on the shoulder, hip, knee and elbow.
Possible pain change measured by a pressure algometry test
Possible pain change measured by a pressure algometry test performed on the shoulder, hip, knee and elbow.
Subjective experience of pain measured using Numeric Rating Scale (NRS)
Subjective experience of pain measured using Numeric Rating Scale (NRS) 0-10 where 0 is the best outcome .
Possible pain change measured using Numeric Rating Scale (NRS) 0-10
Possible pain change measured using Numeric Rating Scale (NRS) 0-10 where 0 is the best outcome .
Ratings of expectation, desire for relief, using Numeric Rating Scale (NRS)
Ratings of expectation, desire for relief, using Numeric Rating Scale (NRS) 0-10 where 0 is the best outcome.
Ratings of expectation, pain variability, using Numeric Rating Scale (NRS) 0-10
Ratings of expectation, pain variability, using Numeric Rating Scale (NRS) 0-10 where 0 is the best outcome.
Activity level, assessed using questionnaire McGills Pain Questionnaire (MPQ).
Activity level are assessed using questionnaire McGills Pain Questionnarie (MPQ). Short version score 0-45.
Quality of Life are assessed using questionnaires RAND-36.
Quality of life are assessed using questionnaires RAND-36 score 0-100
Experience of the effect of the drug, assessed using questionnaire Patients´ Global Impression of Change (PGIC).
Experience of the effect of the drug, score 1-7
Cobalamin in plasma
Control of vitamin B12 is done by measuring cobalamin in plasma.
Lived experiences of pain, health, suffering and well-being.
Qualitative in-depth interviews will be conducted to capture women's lived experiences of pain, health, suffering and well-being.

Full Information

First Posted
June 30, 2021
Last Updated
August 20, 2021
Sponsor
Linnaeus University
Collaborators
Landstinget i Kalmar Län, Region Östergötland, Karolinska Institutet, Kronoberg County Council
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1. Study Identification

Unique Protocol Identification Number
NCT05008042
Brief Title
Evaluation of the Efficiacy of Mecobalamine in the Treatment of Long-term Pain in Women Diagnosed With Fibromyalgia
Official Title
Evaluation of the Efficiacy of Mecobalamine (Vit B12) in the Treatment of Long-term Pain in Women Diagnosed With Fibromyalgia: Single-blind Randomized Controlled Trial With Three-month Follow up
Study Type
Interventional

2. Study Status

Record Verification Date
August 2021
Overall Recruitment Status
Recruiting
Study Start Date
February 6, 2019 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Linnaeus University
Collaborators
Landstinget i Kalmar Län, Region Östergötland, Karolinska Institutet, Kronoberg County Council

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
Fibromyalgia causes long term pain where mostly women are affected. It is not entirely clear how vitamin B12 affects the human pain system, there are however many primary studies that indicate different interesting approaches. Considering that the receptor of NMDA is involved in both long-term pain and vitamin B12 deficiency its of most importance to evaluate whether vitamin B12 decreases the pain sensitivity and the experience of pain i.e hyperalgesia and allodynia, at persons with fibromyalgia.The aim of this study is therefore to evaluate the effect of Mecobalamin (vitamin B12), and describe lived experiences of pain, health, suffering and well-being in women with diagnosed fibromyalgia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fibromyalgia
Keywords
Fibromyalgia,, Chronic pain,, Mekobalamin,, Randomized Controlled Trial, VitaminB12

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial with Three-month follow up
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Mecobalamine 5 mg/ml
Arm Type
Active Comparator
Arm Description
The active substance of vitamin B12 given in the study is Mecobalamin 5mg / ml 2 ml ie 10 mg and is given intramuscularly.
Arm Title
NaCl 9mg/ml
Arm Type
Placebo Comparator
Arm Description
Placebo substance given in the study is Sodium Chloride (NaCL) 9 mg / ml 2 ml, isotonic solution for parenteral use (Baxter) given intramuscularly.
Intervention Type
Drug
Intervention Name(s)
Mecobalamin 5 MG
Intervention Description
The Active substance of vitamin B12 is Mecobalamin 5 mg/ml is given intramuscularly
Intervention Type
Other
Intervention Name(s)
Placebo Comparator : NaCl 9 mg/ml
Intervention Description
Sodium Chloride (NaCL) 9 mg / ml 2 ml, isotonic solution for parenteral use (Baxter) is given intramuscularly.
Primary Outcome Measure Information:
Title
Tolerance time
Description
Primary outcome is tolerance time, maximized to Three minutes, tested using the Cold Pressure test
Time Frame
24 weeks
Secondary Outcome Measure Information:
Title
Pain experience measured by a pressure algometry test
Description
Pain experience measured by a pressure algometry test performed on the shoulder, hip, knee and elbow.
Time Frame
24 weeks
Title
Possible pain change measured by a pressure algometry test
Description
Possible pain change measured by a pressure algometry test performed on the shoulder, hip, knee and elbow.
Time Frame
24 weeks
Title
Subjective experience of pain measured using Numeric Rating Scale (NRS)
Description
Subjective experience of pain measured using Numeric Rating Scale (NRS) 0-10 where 0 is the best outcome .
Time Frame
24 weeks
Title
Possible pain change measured using Numeric Rating Scale (NRS) 0-10
Description
Possible pain change measured using Numeric Rating Scale (NRS) 0-10 where 0 is the best outcome .
Time Frame
24 weeks
Title
Ratings of expectation, desire for relief, using Numeric Rating Scale (NRS)
Description
Ratings of expectation, desire for relief, using Numeric Rating Scale (NRS) 0-10 where 0 is the best outcome.
Time Frame
24 weeks
Title
Ratings of expectation, pain variability, using Numeric Rating Scale (NRS) 0-10
Description
Ratings of expectation, pain variability, using Numeric Rating Scale (NRS) 0-10 where 0 is the best outcome.
Time Frame
24 weeks
Title
Activity level, assessed using questionnaire McGills Pain Questionnaire (MPQ).
Description
Activity level are assessed using questionnaire McGills Pain Questionnarie (MPQ). Short version score 0-45.
Time Frame
24 weeks
Title
Quality of Life are assessed using questionnaires RAND-36.
Description
Quality of life are assessed using questionnaires RAND-36 score 0-100
Time Frame
24 weeks
Title
Experience of the effect of the drug, assessed using questionnaire Patients´ Global Impression of Change (PGIC).
Description
Experience of the effect of the drug, score 1-7
Time Frame
24 weeks
Title
Cobalamin in plasma
Description
Control of vitamin B12 is done by measuring cobalamin in plasma.
Time Frame
24 weeks
Title
Lived experiences of pain, health, suffering and well-being.
Description
Qualitative in-depth interviews will be conducted to capture women's lived experiences of pain, health, suffering and well-being.
Time Frame
24 weeks

10. Eligibility

Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women aged 20-70 years Swedish-speaking Diagnosis of fibromyalgia Safe method of contraception Cobalamin / p (vitamin B12) should be >250 pmol/L < 800 pmol/L Given consent to participate. Exclusion Criteria: Previous treatment with B12 Known hypersensitivity to the active substance Mecobalamin or an additive Vegan as veganism can lead to B12 deficiency Neuroleptics Known heart, kidney or liver disease Reynaud's phenomenon (white fingers) Known neuropathy (impaired sensation) Breastfeeding Pregnancy or plan pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Carina Elmqvist, Ass prof
Phone
+46772288000
Email
carina.elmqvist@lnu.se
First Name & Middle Initial & Last Name or Official Title & Degree
Karin Säll Hansson, Master of sc
Phone
+46772288000
Email
karin.sall_hansson@lnu.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Carina Elmqvist, Ass prof
Organizational Affiliation
Linnaeus University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Linnaeus University
City
Växjö
State/Province
Kronoberg
ZIP/Postal Code
352 91
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Carina Elmqvist, Ass prof
Phone
+46772288000
Email
carina.elmqvist@lnu.se

12. IPD Sharing Statement

Learn more about this trial

Evaluation of the Efficiacy of Mecobalamine in the Treatment of Long-term Pain in Women Diagnosed With Fibromyalgia

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