Neuroprotective Effect of Vitamin B12 and Vitamin B6 Against Vincristine Induced Peripheral Neuropathy
Primary Purpose
Vincristine Induced Peripheral Neuropathy (VIPN)
Status
Completed
Phase
Phase 4
Locations
Bangladesh
Study Type
Interventional
Intervention
Injection Mecobalamin,
Tablet Pyridoxine hydrochloride
Intravenous normal saline 1 ml
Placebo pill
Sponsored by
About this trial
This is an interventional prevention trial for Vincristine Induced Peripheral Neuropathy (VIPN)
Eligibility Criteria
Inclusion Criteria:
- All patients, 18 years of age or older with newly diagnosed ALL going to start induction chemotherapy with Vincristine
- Patients with good performance status (ECOG 0- 3)
- Patients with no preexisting peripheral neuropathy
- Patients with grade 0 neuropathy on admission
- Patients with normal renal function (Serum creatinine <1.5 mg/dl)
- Patients agree to participate in the study signing an informed written consent
Exclusion Criteria:
- Pregnant women and nursing mothers
- Patients with clinical neuropathy due to diabetes mellitus or other causes
- Patients with head neck tumors
- Patients taking anticonvulsants, antidepressants, opioids, vitamin E and other neuropathic pain medication agents
Sites / Locations
- Bangabandhu Sheikh Mujib Medical University
- Dhaka Medical College Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Placebo Comparator
Arm Label
Experimental
Placebo
Arm Description
Intervention: Injection Mecobalamin (500mcg) three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks. Intervention: Tablet Pyridoxine hydrochloride (25 mg) 2 tablets thrice daily for 5 weeks.
Intervention: Injection normal saline (1 ml) three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks. Intervention: Oral placebo pill 2 tablets thrice daily for 5 weeks.
Outcomes
Primary Outcome Measures
Time of onset of Vincristine Induced Peripheral Neuropathy
Severity of Vincristine Induced Peripheral Neuropathy
Incidence of Vincristine Induced Peripheral Neuropathy
Secondary Outcome Measures
Full Information
NCT ID
NCT02923388
First Posted
August 31, 2016
Last Updated
November 6, 2019
Sponsor
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
1. Study Identification
Unique Protocol Identification Number
NCT02923388
Brief Title
Neuroprotective Effect of Vitamin B12 and Vitamin B6 Against Vincristine Induced Peripheral Neuropathy
Official Title
Neuroprotective Effect of Vitamin B12 and Vitamin B6 Against Vincristine Induced Peripheral Neuropathy: A Randomized, Double Blind, Placebo Controlled, Multi Center Trial
Study Type
Interventional
2. Study Status
Record Verification Date
November 2019
Overall Recruitment Status
Completed
Study Start Date
October 2016 (undefined)
Primary Completion Date
June 2018 (Actual)
Study Completion Date
July 2018 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study will be conducted to evaluate the effect of vitamin B12 and vitamin B6 in delaying the onset and reducing the incidence and severity of Vincristine Induced Peripheral Neuropathy (VIPN) in Acute Lymphoblastic Leukemia (ALL) patient.
Detailed Description
Acute Lymphoblastic Leukemia (ALL) is an emerging health burden for Bangladesh. It is anticipated that about 20 million people are going to be affected annually by 2025 in countries currently on developmental transition. Good prognostic outcome of ALL relies on uninterrupted and complete course of chemotherapy. About 85% of adult patients and 98% of children attain complete recovery with full course of treatment. One of the crucial chemotherapeutic agents used to treat ALL is vincristine. It is needed to complete vincristine with adequate dose in order to get a better prognostic outcome. About 45% of the patients getting vincristine develop a deleterious side effect called Vincristine Induced Peripheral Neuropathy (VIPN). Unfortunately, development of VIPN results in dose reduction, protocol deviation and even abandonment of treatment with vincristine in some ALL patients. Better prognostic outcome becomes an arcadia. So far, many researches have been conducted to explore a way to prevent or treat VIPN. But still no conclusive recommendation can be made. Therefore, VIPN has become an important issue need to be addressed. This study will be a small effort to identify the potential of vitamin B12 and vitamin B6 as probable preventive measures of VIPN. Evidence suggests that, vitamin B12 and vitamin B6 two water soluble, non toxic vitamins well recognized for the treatment of peripheral neuropathy. Vitamin B12 plays a very fundamental role in neurological function. It exerts its physiological effects through mediating two principal enzymatic pathways by which it maintains the integrity of neuronal membrane. On the other hand, vitamin B6 or pyridoxine is an essential co- factor in various synthesis pathways including synthesis of myelin sheath. Patients will be randomly allocated into two arms by using online research randomizer and newly diagnosed ALL patients will be enrolled in this research. From the day of starting chemotherapy, patients on arm A (Intervention arm) will be concurrently administered with vitamin B12 and vitamin B6. Vitamin B12 will be given 500 μg three times a week intravenously on a basis of every alternate day except the day of receiving vincristine and vitamin B6 will be given 50 mg thrice daily orally during the induction period (5 weeks) of chemotherapy cycle. On the other hand, patients on arm B (Placebo arm) will be given placebo pill and intravenous placebo injection at same interval. Prior to initiation of induction chemotherapy each participant will undergo neuropathy evaluation per National Cancer Institute's Common Terminology Criteria for Adverse Events (NCI-CTCAE) v.4.0 scale and will be interviewed according to the neurotoxicity subscale of Functional Assessment of Cancer Therapy (FACT) -GOG- Ntx quality of life assessment questionnaire. The participants will be re-evaluated once weekly on the outset of 2nd week, 3rd week, 4th and 5th week of vincristine chemotherapy during induction period. They will be assessed per NCI-CTCAE v.4.0 scale for severity of neuropathy and by FACT- GOG- Ntx by answering specific questions regarding the presence of tingling, numbness, pain, muscle weakness and motor activities. As neuropathy and neuropathic pain are mostly subjective issue rather than objective and reflected more comprehensively by the particular person encountering with, so patient based measures will be used in this study. Incidence, onset and severity of peripheral neuropathy will be compared on both arms.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vincristine Induced Peripheral Neuropathy (VIPN)
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
88 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Experimental
Arm Type
Active Comparator
Arm Description
Intervention: Injection Mecobalamin (500mcg) three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks.
Intervention: Tablet Pyridoxine hydrochloride (25 mg) 2 tablets thrice daily for 5 weeks.
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Intervention: Injection normal saline (1 ml) three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks.
Intervention: Oral placebo pill 2 tablets thrice daily for 5 weeks.
Intervention Type
Drug
Intervention Name(s)
Injection Mecobalamin,
Other Intervention Name(s)
Vitamin B12
Intervention Description
Injection Mecobalamin (500mcg) three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks.
Intervention Type
Drug
Intervention Name(s)
Tablet Pyridoxine hydrochloride
Other Intervention Name(s)
Vitamin B6
Intervention Description
Tab. Pyridoxine hydrochloride (25 mg) 2 tablets thrice daily for 5 weeks
Intervention Type
Drug
Intervention Name(s)
Intravenous normal saline 1 ml
Other Intervention Name(s)
Normal saline
Intervention Description
Normal saline 1 ml three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks
Intervention Type
Drug
Intervention Name(s)
Placebo pill
Other Intervention Name(s)
Placebo
Intervention Description
Placebo pill orally thrice daily for 5 weeks
Primary Outcome Measure Information:
Title
Time of onset of Vincristine Induced Peripheral Neuropathy
Time Frame
0 weeks (baseline), change in neuropathy status on the outset 2nd week, 3rd week, 4th week and 5th week of vincristine chemotherapy
Title
Severity of Vincristine Induced Peripheral Neuropathy
Time Frame
On the outset of 1st week change in the severity of neuropathy on the outset of 2nd week, 3rd week, 4th week, 5th week of vincristine chemotherapy
Title
Incidence of Vincristine Induced Peripheral Neuropathy
Time Frame
Cumulative incidence at 5th week of vincristine chemotherapy
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All patients, 18 years of age or older with newly diagnosed ALL going to start induction chemotherapy with Vincristine
Patients with good performance status (ECOG 0- 3)
Patients with no preexisting peripheral neuropathy
Patients with grade 0 neuropathy on admission
Patients with normal renal function (Serum creatinine <1.5 mg/dl)
Patients agree to participate in the study signing an informed written consent
Exclusion Criteria:
Pregnant women and nursing mothers
Patients with clinical neuropathy due to diabetes mellitus or other causes
Patients with head neck tumors
Patients taking anticonvulsants, antidepressants, opioids, vitamin E and other neuropathic pain medication agents
Facility Information:
Facility Name
Bangabandhu Sheikh Mujib Medical University
City
Dhaka
Country
Bangladesh
Facility Name
Dhaka Medical College Hospital
City
Dhaka
Country
Bangladesh
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Neuroprotective Effect of Vitamin B12 and Vitamin B6 Against Vincristine Induced Peripheral Neuropathy
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