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Efficacy and Safety of Nerve Growth Factor or Edaravone on Alcohol-induced Brain Injury

Efficacy and Safety of Nerve Growth Factor or Edaravone on Alcohol-induced Brain Injury

Status
UNKNOWN
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03968042
Enrollment
150
Registered
2019-05-30
Start date
2019-06-30
Completion date
2021-12-31
Last updated
2020-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alcohol-induced Brain Injury

Keywords

Alcohol-induced brain injury, atrophy, demyelination

Brief summary

Alcohol is one of most common harmful substance, and alcohol intake brings great burden on health worldwide. Excess alcohol intake may lead to alcohol-related brain injuries and cognitive impairment. Although both nerve growth factor and antioxidative treatment were effective to relieve alcohol-related injuries in central nervous system in the preclinical studies, there is no relevant clinical trial about their efficacy and safety on patients. Since nerve growth factor and one of the antioxidative medication, edaravone, have been used in some neural diseases in clinical trials, we tend to evaluate the efficacy and safety of nerve growth factor, or edaravone on alcohol-induced brain injuries. The study is a randomized-controlled study and the patients will be assigned into one of the following three groups randomly: (1) regular treatment (combination of vitamin B1, B6, C, E and mecobalamine) with nerve growth factor for 2 weeks and subsequently regular treatment for 6 months; (2) regular treatment (RT) with edaravone for 2 weeks and subsequently RT for 6 months; (3) RT alone for 6 months. The patients will be followed up for 6 months. Cognitive functions, recurrence of alcohol dependence, duration of abstention, alcohol intake, craving for alcohol and other psychological assessments will be recorded and compared among the 3 treatment groups and the efficacy of nerve growth factor or edaravone will be evaluated in our study.

Interventions

Intramuscular injection for 2 weeks

Intravenous injection for 2 weeks

DRUGCombination of vitamin B1, B6, C, E and mecobalamine

Medications of combination of vitamin B1, B6, C, E and mecobalamine for 6 months

Sponsors

Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosis as alcohol dependence according to DSM-IV criteria * MRI-proved demyelinating lesions or atrophy in the brain of the patient * No definite history of neurological diseases and psychological problems * Volunteer to participate the study, cooperate to be followed up

Exclusion criteria

* Acute withdrawal state and CIWA score \> 9 * With other neurological diseases and psychological problems * With ever brain trauma and damage * With other psychological medications or other substance dependence

Design outcomes

Primary

MeasureTime frameDescription
Cognitive improvement2 weeksExecutive function by digit symbol substitute test (DSST) ranging from 0 to 90. Higher score indicates better executive function.
Cognitive assessment3 monthsCognitive assessment by Montreal Cognitive Assessment (MoCA) ranging from 0 to 30. Lower score indicates worse cognitive function.

Secondary

MeasureTime frameDescription
Alcohol intake2 weeks, 2 months, 3 months, 6 monthsDiaries of alcohol intake in different time of the follow ups
Craving for alcohol2 weeks, 2 months, 3 months, 6 monthsCraving assessment for alcohol by Obsessive Compulsive Drinking Scale (OCDS) ranging from 0 to 40. Higher score of OCDS indicates more desire for alcohol.
The rate of relapse of alcohol dependence after discharge from hospital2 monthsRecurrence of alcohol dependence
Psychological assessment - Depression2 weeks, 2 months, 3 months, 6 monthsPsychological assessment by Patient Health Questionnaire-9 (PHQ-9) ranging from 0 to 27. Higher score indicates more severer depression.
Psychological assessment - Sleep2 weeks, 2 months, 3 months, 6 monthsPsychological assessment by Pittsburgh Sleep Quality Index (PSQI) ranging from 0 to 21. Higher score indicates worse sleep.
Psychological assessment - Anxiety2 weeks, 2 months, 3 months, 6 monthsPsychological assessment by Generalized Anxiety Disorder-7 (GAD-7) ranging from 0 to 21. Higher score indicates more severer anxiety.
Duration of abstinence6 monthsThe total time or period without any intake of alcohol during follow ups

Countries

China

Contacts

Primary ContactYing Peng, MD, PhD
pengy2@mail.sysu.edu.cn+86-13380051581
Backup ContactHongxuan Wang, MD, PhD
wanghx8@mail.sysu.edu.cn+86-13824498978

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026