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Vincristine Induced Peripheral Neuropathy (VIPN)Phase 4NCT02923388

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

A Phase 4 study testing Injection Mecobalamin,, Tablet Pyridoxine hydrochloride and Intravenous normal saline 1 ml in people with Vincristine Induced Peripheral Neuropathy (VIPN), run by Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh at 2 sites in Bangladesh.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial 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 more about this study

Who is it for?
Ages 18 to 90 years
What is being tested?
Injection Mecobalamin,, Tablet Pyridoxine hydrochloride and Intravenous normal saline 1 ml
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
88 participants
Where
2 sitesBangladesh
Study dates
Oct 2016to Jul 2018
Phase
Phase 4
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 90 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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

Who cannot join

  • 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

Trial locations and contacts

2 sites in 1 country.

Bangladesh2 sites
  • Bangabandhu Sheikh Mujib Medical University

    Dhaka

  • Dhaka Medical College Hospital

    Dhaka

Other trials in Bangladesh

About this study

Official title: Neuroprotective Effect of Vitamin B12 and Vitamin B6 Against Vincristine Induced Peripheral Neuropathy: A Randomized, Double Blind, Placebo Controlled, Multi Center Trial

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.

Being tested
Injection Mecobalamin,, Tablet Pyridoxine hydrochloride, Intravenous normal saline 1 ml, Placebo pill

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Injection Mecobalamin,Drug

    Also called Vitamin B12

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

  • Tablet Pyridoxine hydrochlorideDrug

    Also called Vitamin B6

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

  • Intravenous normal saline 1 mlDrug

    Also called Normal saline

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

  • Placebo pillDrug

    Also called Placebo

    Placebo pill orally thrice daily for 5 weeks

Study groups in NCT02923388
Study groupRoleWhat they receive
ExperimentalActive comparatorIntervention: 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.
Receives: Drug: Injection Mecobalamin,; Drug: Tablet Pyridoxine hydrochloride
PlaceboPlacebo comparatorIntervention: 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.
Receives: Drug: Intravenous normal saline 1 ml; Drug: Placebo pill

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Time of onset of Vincristine Induced Peripheral Neuropathy

    Measured: 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

    Measured: 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

    Measured: Cumulative incidence at 5th week of vincristine chemotherapy

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Oct 2016 (estimated)
  2. Study startOct 2016
  3. Primary completionJun 2018
  4. Study completionJul 2018

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Prevention
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
88 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02923388
Sponsor's protocol ID
No. BSMMU/2016/8305
Status last verified
Nov 2019
First submitted
31 Aug 2016
Last updated
8 Nov 2019
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A Phase 4 study testing Injection Mecobalamin,, Tablet Pyridoxine hydrochloride and Intravenous normal saline 1 ml in people with Vincristine Induced Peripheral Neuropathy (VIPN), run by Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh at 2 sites in Bangladesh.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 8 Nov 2019. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 2 sites in Bangladesh. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 4 studies take place after a treatment is approved, to learn more about its long-term benefits and risks in everyday use.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

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). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 8 Nov 2019.

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