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

Sponsor
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University (Other)
Overall Status
Recruiting
CT.gov ID
NCT03968042
Collaborator
(none)
150
1
3
29.1
5.2

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Drug: Nerve Growth Factor
  • Drug: Edaravone
  • Drug: Combination of vitamin B1, B6, C, E and mecobalamine
Phase 2

Study Design

Study Type:
Interventional
Anticipated Enrollment :
150 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Efficacy and Safety of Nerve Growth Factor or Edaravone on Alcohol-induced Brain Injury
Actual Study Start Date :
Jun 30, 2019
Anticipated Primary Completion Date :
Dec 1, 2021
Anticipated Study Completion Date :
Dec 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Placebo Comparator: Regular treatment (RT)

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

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

Experimental: RT with NGF

Nerve growth factor adding to regular treatment

Drug: Nerve Growth Factor
Intramuscular injection for 2 weeks

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

Experimental: RT with EDV

Edaravone adding to regular treatment

Drug: Edaravone
Intravenous injection for 2 weeks

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

Outcome Measures

Primary Outcome Measures

  1. Cognitive improvement [2 weeks]

    Executive function by digit symbol substitute test (DSST) ranging from 0 to 90. Higher score indicates better executive function.

  2. Cognitive improvement [2 months]

    Executive function by digit symbol substitute test (DSST) ranging from 0 to 90. Higher score indicates better executive function.

  3. Cognitive improvement [3 months]

    Executive function by digit symbol substitute test (DSST) ranging from 0 to 90. Higher score indicates better executive function.

  4. Cognitive improvement [6 months]

    Executive function by digit symbol substitute test (DSST) ranging from 0 to 90. Higher score indicates better executive function.

  5. Cognitive assessment [3 months]

    Cognitive assessment by Montreal Cognitive Assessment (MoCA) ranging from 0 to 30. Lower score indicates worse cognitive function.

  6. Cognitive assessment [6 months]

    Cognitive assessment by Montreal Cognitive Assessment (MoCA) ranging from 0 to 30. Lower score indicates worse cognitive function.

Secondary Outcome Measures

  1. The rate of relapse of alcohol dependence after discharge from hospital [2 months]

    Recurrence of alcohol dependence

  2. Duration of abstinence [6 months]

    The total time or period without any intake of alcohol during follow ups

  3. Alcohol intake [2 weeks, 2 months, 3 months, 6 months]

    Diaries of alcohol intake in different time of the follow ups

  4. Craving for alcohol [2 weeks, 2 months, 3 months, 6 months]

    Craving assessment for alcohol by Obsessive Compulsive Drinking Scale (OCDS) ranging from 0 to 40. Higher score of OCDS indicates more desire for alcohol.

  5. Psychological assessment - Anxiety [2 weeks, 2 months, 3 months, 6 months]

    Psychological assessment by Generalized Anxiety Disorder-7 (GAD-7) ranging from 0 to 21. Higher score indicates more severer anxiety.

  6. Psychological assessment - Depression [2 weeks, 2 months, 3 months, 6 months]

    Psychological assessment by Patient Health Questionnaire-9 (PHQ-9) ranging from 0 to 27. Higher score indicates more severer depression.

  7. Psychological assessment - Sleep [2 weeks, 2 months, 3 months, 6 months]

    Psychological assessment by Pittsburgh Sleep Quality Index (PSQI) ranging from 0 to 21. Higher score indicates worse sleep.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sun Yat-sen Memorial Hospital, Sun Yat-sen University Guangzhou Guangdong China

Sponsors and Collaborators

  • Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Ying Peng, Professor, Director of Department of Neurology, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
ClinicalTrials.gov Identifier:
NCT03968042
Other Study ID Numbers:
  • 2019-13-NGF-EDV
First Posted:
May 30, 2019
Last Update Posted:
Oct 27, 2020
Last Verified:
Oct 1, 2020
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Ying Peng, Professor, Director of Department of Neurology, Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 27, 2020