Vitamin B12 vs B3 for Nerve Regeneration and Functional Recovery After Pediatric Traumatic Brain Injury

Sponsor
KRL Hospital, Islamabad (Other)
Overall Status
Completed
CT.gov ID
NCT05958277
Collaborator
(none)
300
1
2
20.1
14.9

Study Details

Study Description

Brief Summary

A traumatic brain injury (TBI) is among the most frequent reasons for neurological impairment in young people. The investigators investigated whether vitamin B12 vs B3 therapy could reduce the severity of traumatic brain injury (TBI) due to their positive effects on axon regrowth following nerve damage. The method utilized was a series of non-random samples. With a 95% confidence interval and a 5% margin of error, a total sample of 300 patients was estimated using Epi Info. Participants in our study comprised both boys and girls with severe TBI ages 6 to 15 years old.

Two groups of 300 children were recruited. B3 (16 mg/day) was administered to group 1 and B12 (125-250 mcg/day) was provided to group 2. It is evaluated through follow-ups on a range of tests to evaluate cognitive capacity, sensorimotor activity and staircase test (working and reference memory). Pre-and post-treatment GCS measurements were conducted. Three weeks and a year following the treatment of TBI, children underwent neurobehavioral testing. The measurement of gait analysis was done. The standard error and mean of statistically examined data were shown by paired t-test.

Condition or Disease Intervention/Treatment Phase
  • Drug: Vitamin B3
  • Drug: Vitamin B12
Phase 3

Detailed Description

A traumatic brain injury (TBI) is among the most frequent reasons for neurological impairment in young people. The investigators investigated whether vitamin B12 vs B3 therapy could reduce the severity of traumatic brain injury (TBI) due to their positive effects on axon regrowth following nerve damage. The method utilized was a series of non-random samples. With a 95% confidence interval and a 5% margin of error, a total sample of 300 patients was estimated using Epi Info. Participants in our study comprised both boys and girls with severe TBI ages 6 to 15 years old.

Two groups of 300 children were recruited. B3 (16 mg/day) was administered to group 1 and B12 (125-250 mcg/day) was provided to group 2. It is evaluated through follow-ups on a range of tests to evaluate cognitive capacity, sensorimotor activity and staircase test (working and reference memory). Pre-and post-treatment GCS measurements were conducted. Three weeks and a year following the treatment of TBI, children underwent neurobehavioral testing. The measurement of gait analysis was done. The standard error and mean of statistically examined data were shown by paired t-test.

Study Design

Study Type:
Interventional
Actual Enrollment :
300 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Vitamin B12 vs B3 for Nerve Regeneration and Functional Recovery After Pediatric Traumatic Brain Injury
Actual Study Start Date :
Jun 1, 2021
Actual Primary Completion Date :
Jan 28, 2023
Actual Study Completion Date :
Feb 3, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Vitamin B3

Vitamin B3 group

Drug: Vitamin B3
Vitamin B3 upto 16 mg/day

Experimental: Vitamin B12 group

Vitamin B12 group

Drug: Vitamin B12
Vit B12 upto 250 mcg per day

Outcome Measures

Primary Outcome Measures

  1. Change in Stair Climb Test (SCT) score [18 months]

    The stair test is a measurement of functional strength, balance, and agility achieved by ascending and descending a specific number of steps. Scoring involves recording the total time taken to ascend and descend the steps to the nearest 100th of a second. Lower values indicate better performance.

Eligibility Criteria

Criteria

Ages Eligible for Study:
6 Years to 15 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Children aged 6 to 15 years old

  • Children with severe TBI of

  • Children of both genders

Exclusion Criteria:
  • Those with mild injury

  • Stable Glasgow Coma Scale

  • Not willing to consent

Contacts and Locations

Locations

Site City State Country Postal Code
1 KRL Hospital Islamabad Pakistan

Sponsors and Collaborators

  • KRL Hospital, Islamabad

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Hassan Mumtaz, Principal Researcher, KRL Hospital, Islamabad
ClinicalTrials.gov Identifier:
NCT05958277
Other Study ID Numbers:
  • KRL/02/19/2
First Posted:
Jul 24, 2023
Last Update Posted:
Jul 24, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 24, 2023