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CompletedNCT02923388Updated Nov 8, 2019

Neuroprotective Effect of Vitamin B12 and Vitamin B6 Against Vincristine Induced Peripheral Neuropathy

A Phase 4 interventional study of Injection Mecobalamin, and Tablet Pyridoxine hydrochloride in Vincristine Induced Peripheral Neuropathy (VIPN), sponsored by Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh. Completed at 2 sites in Bangladesh. Open to participants aged 18 Years to 90 Years. Per ClinicalTrials.gov, last updated 2019-11-08.

Sponsored by Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh · Phase 4, Interventional, and Prevention

Phase
Phase 4
Study type
Interventional
Enrollment
88
Allocation
Randomized
Ages
18 Years to 90 Years
Sex
All
01

Study 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.

Read the 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.

02

Conditions studied

  • Vincristine Induced Peripheral Neuropathy (VIPN)
03

In context

Peripheral Nervous System Diseases

1,003 studies on the registry are indexed under Peripheral Nervous System Diseases; 177 are open to participants now.

This study's enrollment of 88 is above the median of 60 across 768 interventional studies indexed under Peripheral Nervous System Diseases.

Browse Peripheral Nervous System Diseases studies →

Lead sponsor

Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh is the lead sponsor of 126 studies on the registry; 24 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 90 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. All patients, 18 years of age or older with newly diagnosed ALL going to start induction chemotherapy with Vincristine
  2. Patients with good performance status (ECOG 0- 3)
  3. Patients with no preexisting peripheral neuropathy
  4. Patients with grade 0 neuropathy on admission
  5. Patients with normal renal function (Serum creatinine \<1.5 mg/dl)
  6. Patients agree to participate in the study signing an informed written consent

Exclusion criteria

Exclusion Criteria:

  1. Pregnant women and nursing mothers
  2. Patients with clinical neuropathy due to diabetes mellitus or other causes
  3. Patients with head neck tumors
  4. Patients taking anticonvulsants, antidepressants, opioids, vitamin E and other neuropathic pain medication agents
05

Study design

Phase
Phase 4
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Quadruple (Participant, Care provider, Investigator, Outcomes assessor)
Enrollment
88 participants (actual)

Study arms

  • Active comparator
    Experimental

    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.

    Drug: Injection Mecobalamin, · Drug: Tablet Pyridoxine hydrochloride

  • Placebo comparator
    Placebo

    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.

    Drug: Intravenous normal saline 1 ml · Drug: Placebo pill

Interventions

  • DrugInjection Mecobalamin,

    Injection Mecobalamin (500mcg) three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks.

    Also known as: Vitamin B12

  • DrugTablet Pyridoxine hydrochloride

    Tab. Pyridoxine hydrochloride (25 mg) 2 tablets thrice daily for 5 weeks

    Also known as: Vitamin B6

  • DrugIntravenous normal saline 1 ml

    Normal saline 1 ml three times a week (day 1, 3 and 5 of vincristine chemotherapy) for 5 weeks

    Also known as: Normal saline

  • DrugPlacebo pill

    Placebo pill orally thrice daily for 5 weeks

    Also known as: Placebo

06

What researchers measure

Primary outcomes

  1. 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

  2. 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

  3. Incidence of Vincristine Induced Peripheral Neuropathy

    Time frame: Cumulative incidence at 5th week of vincristine chemotherapy

07

Study locations

2 sites
  • Bangabandhu Sheikh Mujib Medical University
    Dhaka, Bangladesh
  • Dhaka Medical College Hospital
    Dhaka, Bangladesh
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 8, 2019, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02923388
Lead sponsor
Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
Responsible party
Fatiha Tasmin Jeenia (Resident, Department of Pharmacology, BSMMU, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh) — Principal investigator
First posted
Oct 4, 2016
Start date
Oct 2016
Primary completion
Jun 2018
Completion
Jul 2018
Last update
Nov 8, 2019

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Nov 2019. You cannot join it, but the record below documents what was studied.

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