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Clinical Study of Ligustrazine in Treating Alcohol Addiction

Primary Purpose

Alcohol Abuse, Arteriosclerosis

Status
Recruiting
Phase
Phase 4
Locations
China
Study Type
Interventional
Intervention
Ligustrazine by intravenously administration
Ligustrazine by mouth
Placebo by intravenously administration
Placebo by mouth
Sponsored by
Shenzhen Kangning Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Alcohol Abuse focused on measuring Alcohol, Addiction, Arteriosclerosis, Ligustrazine

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Alcohol addiction: ①Aged 18~65 years old; ② Meet the diagnostic criteria of DSM-IV alcohol dependence; ③No clear history of neurological diseases in the past, no family history of mental diseases; ④Voluntary participation in research, with good follow-up and observation, and good compliance; ⑤ No obvious psychotic symptoms. Combined with the therapeutic indications of ligustrazine, selected cases must meet any of the following criteria on the premise of normal coagulation routine (no bleeding tendency): D-2 polymer ≥500 (thrombotic tendency) or atherosclerosis index ≥4 or one or more blood lipid indicators (TC, HDL, LDL) are abnormal. Arteriosclerosis index (AI) = [total cholesterol (TC) - high-density lipoprotein (HDL)] ÷ high-density lipoprotein (HDL), the normal value of AI is <4, reflecting that the degree of arteriosclerosis is not serious or mild, The smaller the value, the lighter the degree of arteriosclerosis. If the arteriosclerosis index ≥ 4, it means that obvious arteriosclerosis has occurred, and the larger the value, the more serious the degree of arteriosclerosis. Exclusion Criteria: ① Acute alcohol withdrawal phase, CIWA-Ar > 9 points; Severe neurological or mental diseases caused by diseases other than chronic alcohol dependence: such as stroke, intracranial infection, brain tumor, schizophrenia, etc.; Have experienced traumatic brain injury or other damage to brain tissue; ④ Taking any other psychotropic drugs, drug use or other substance dependence in the short term; ⑤ There are contraindications to the application of ligustrazine, or women are pregnant and other conditions that are not suitable for drug use; ⑥ There are conditions that are not suitable for head MRI examination, such as claustrophobia, metal objects in the body, etc.

Sites / Locations

  • Shenzhen Kangning HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Placebo Comparator

Experimental

Experimental

Arm Label

Placebo

Ligustrazine short-term treatment

Ligustrazine maintenance treatment

Arm Description

Enrolled participants would accept intravenous administration of 250ml saline per day for 15 days, then 50 mg placebo tablet by mouth would be maintained for 1 year.

Ligustrazine hydrochloride was administered intravenously by dissolving 40mg in 250ml saline per day for 15 days. Then, a 50 mg placebo tablet by mouth would be maintained for 1 year

Ligustrazine hydrochloride was administered intravenously by dissolving 40mg in 250ml saline per day for 15 days,then, a 50 mg Ligustrazine tablet by mouth would be maintained for 1 year.

Outcomes

Primary Outcome Measures

Relapse rate
Percentage of participants who relapse by assuming that drinking alcohol on more than 3 days in a month in an unrestricted environment is re-drinking

Secondary Outcome Measures

Time to maintain abstinence
Measurement of exactly time(days) to maintain abstinence
Frequency of alcohol consumed
Assessment of frequency to consume alcohol
Amount of alcohol consumed
The amount of alcohol consumed would be measured.
Change from baseline in alcohol craving by using Visual Analog Scale of Alcohol Craving at week 4.
Alcohol-specific Visual Analog Scale is a valid measurements of craving for a alcohol. Possible scores range from 0 (no craving) to 10 (want to drink imediately). Change= (week 4 score - baseline score)
Percent Mean Change in Blood Oxygen-level Dependent (BOLD) Scores
BOLD fMRI signals evaluate different brain ROI

Full Information

First Posted
June 16, 2023
Last Updated
October 12, 2023
Sponsor
Shenzhen Kangning Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT05942352
Brief Title
Clinical Study of Ligustrazine in Treating Alcohol Addiction
Official Title
Clinical Study of Ligustrazine in Treating Alcohol Addiction
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
July 28, 2023 (Actual)
Primary Completion Date
July 2024 (Anticipated)
Study Completion Date
July 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shenzhen Kangning Hospital

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Alcohol consumption is one of the most important risk factors for chronic non-communicable diseases in the population, and it is also the main cause of death from cancer, cardiovascular disease and lung disease, causing serious health, economic and social problems. The current alcohol-abstinence drugs have limited therapeutic effects and still present a high relapse rate. It is an urgent need to develop effective drugs for the treatment of alcohol addiction. The multimodal mechanism of action of ligustrazine in the central nervous system indicates that ligustrazine is expected to be developed as a potential therapeutic drug for alcohol addiction. Our study investigated the therapeutic effect of ligustrazine on subjects with alcohol addiction and the mechanism of multimodal brain imaging by administering ligustrazine, in order to develop new targeted drugs for alcohol treatment and provide more effective diagnosis and treatment methods for clinical treatment.
Detailed Description
Background: Alcohol use disorders (AUD) is a common chronic disease with great harm to society, causing a huge disease burden and social burden. In recent years, a lot of progress has been made in the field of drug abuse in the field of neurobiology, but it is difficult to apply it to AUD. The clinical treatment of alcohol addiction has always been under the predicament of lack of medicine and drugs, and the development of new therapeutic intervention methods is urgently needed. Although the neurobiological mechanism of ligustrazine's efficacy is still unclear, its multimodal mechanism of action in the central nervous system suggests that ligustrazine is expected to be developed as a potential therapeutic drug for alcohol addiction. Objective: This study intends to develop a therapeutic drug that can effectively relieve alcohol withdrawal syndrome, promote the disappearance of addictive behaviors, and effectively prevent re-drinking for the main active ingredient ligustrazine of the traditional Chinese medicine Ligusticum chuanxiong. The implementation of this project will help to expand the new functions (new indications) of traditional Chinese medicine and its main active ingredient ligustrazine, which may be developed into an effective drug for the treatment of alcohol addiction, and explore its neuroimaging mechanism. METHODS: Eligible alcohol addiction cases were recruited and assigned to 3 treatment groups according to randomized double-blind procedure (conventional treatment + placebo control group, conventional treatment + ligustrazine short-term treatment group, conventional treatment + ligustrazine maintenance treatment group ; about 100 cases in each group). After 15 days of group treatment, follow-up for 1 year, observe and compare the relapse rate of alcohol addiction, the duration of abstinence (days), the frequency and amount of drinking, the degree of craving, and other cognitive and psychological changes in each group, and record adverse reactions. Clinical efficacy and safety of ligustrazine on alcohol addiction. The changes of multimodal brain imaging in each group were analyzed, and the neural effects of ligustrazine treatment were explored. ②Recruit healthy controls ≥ 100 cases, match the sex and age with the cases, collect cognitive psychological indicators and brain imaging data at baseline and 1 year after baseline, and compare them in parallel with each treatment group to explore the treatment of alcohol addiction with Ligustrazine neural mechanism.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Alcohol Abuse, Arteriosclerosis
Keywords
Alcohol, Addiction, Arteriosclerosis, Ligustrazine

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
400 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Enrolled participants would accept intravenous administration of 250ml saline per day for 15 days, then 50 mg placebo tablet by mouth would be maintained for 1 year.
Arm Title
Ligustrazine short-term treatment
Arm Type
Experimental
Arm Description
Ligustrazine hydrochloride was administered intravenously by dissolving 40mg in 250ml saline per day for 15 days. Then, a 50 mg placebo tablet by mouth would be maintained for 1 year
Arm Title
Ligustrazine maintenance treatment
Arm Type
Experimental
Arm Description
Ligustrazine hydrochloride was administered intravenously by dissolving 40mg in 250ml saline per day for 15 days,then, a 50 mg Ligustrazine tablet by mouth would be maintained for 1 year.
Intervention Type
Drug
Intervention Name(s)
Ligustrazine by intravenously administration
Other Intervention Name(s)
Tetramethylpyrazine by intravenously administration
Intervention Description
Ligustrazine hydrochloride was administered intravenously by dissolving 40mg in 250ml saline per day for 15 days
Intervention Type
Drug
Intervention Name(s)
Ligustrazine by mouth
Other Intervention Name(s)
Tetramethylpyrazine by mouth
Intervention Description
50 mg Ligustrazine tablet by mouth would be maintained for 1 year
Intervention Type
Drug
Intervention Name(s)
Placebo by intravenously administration
Other Intervention Name(s)
Saline by intravenously administration
Intervention Description
Intravenous administration of 250ml saline per day for 15 days
Intervention Type
Drug
Intervention Name(s)
Placebo by mouth
Other Intervention Name(s)
Starch tablet by mouth
Intervention Description
50 mg placebo tablet by mouth would be maintained for 1 year
Primary Outcome Measure Information:
Title
Relapse rate
Description
Percentage of participants who relapse by assuming that drinking alcohol on more than 3 days in a month in an unrestricted environment is re-drinking
Time Frame
Four week after treatment
Secondary Outcome Measure Information:
Title
Time to maintain abstinence
Description
Measurement of exactly time(days) to maintain abstinence
Time Frame
Four week after treatment
Title
Frequency of alcohol consumed
Description
Assessment of frequency to consume alcohol
Time Frame
Four week after treatment
Title
Amount of alcohol consumed
Description
The amount of alcohol consumed would be measured.
Time Frame
Four week after treatment
Title
Change from baseline in alcohol craving by using Visual Analog Scale of Alcohol Craving at week 4.
Description
Alcohol-specific Visual Analog Scale is a valid measurements of craving for a alcohol. Possible scores range from 0 (no craving) to 10 (want to drink imediately). Change= (week 4 score - baseline score)
Time Frame
Four week after treatment
Title
Percent Mean Change in Blood Oxygen-level Dependent (BOLD) Scores
Description
BOLD fMRI signals evaluate different brain ROI
Time Frame
Four week after treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Alcohol addiction: ①Aged 18~65 years old; ② Meet the diagnostic criteria of DSM-IV alcohol dependence; ③No clear history of neurological diseases in the past, no family history of mental diseases; ④Voluntary participation in research, with good follow-up and observation, and good compliance; ⑤ No obvious psychotic symptoms. Combined with the therapeutic indications of ligustrazine, selected cases must meet any of the following criteria on the premise of normal coagulation routine (no bleeding tendency): D-2 polymer ≥500 (thrombotic tendency) or atherosclerosis index ≥4 or one or more blood lipid indicators (TC, HDL, LDL) are abnormal. Arteriosclerosis index (AI) = [total cholesterol (TC) - high-density lipoprotein (HDL)] ÷ high-density lipoprotein (HDL), the normal value of AI is <4, reflecting that the degree of arteriosclerosis is not serious or mild, The smaller the value, the lighter the degree of arteriosclerosis. If the arteriosclerosis index ≥ 4, it means that obvious arteriosclerosis has occurred, and the larger the value, the more serious the degree of arteriosclerosis. Exclusion Criteria: ① Acute alcohol withdrawal phase, CIWA-Ar > 9 points; Severe neurological or mental diseases caused by diseases other than chronic alcohol dependence: such as stroke, intracranial infection, brain tumor, schizophrenia, etc.; Have experienced traumatic brain injury or other damage to brain tissue; ④ Taking any other psychotropic drugs, drug use or other substance dependence in the short term; ⑤ There are contraindications to the application of ligustrazine, or women are pregnant and other conditions that are not suitable for drug use; ⑥ There are conditions that are not suitable for head MRI examination, such as claustrophobia, metal objects in the body, etc.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaojian Jia, PhD
Phone
+86 138 2379 7115
Email
94205638@qq.com
First Name & Middle Initial & Last Name or Official Title & Degree
Qi Wang, PhD
Phone
+86 13688819667
Email
16981017@qq.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiaojian Jia
Organizational Affiliation
Shenzhen Kangning Hospita
Official's Role
Principal Investigator
Facility Information:
Facility Name
Shenzhen Kangning Hospital
City
Shenzhen
State/Province
Guangdong
ZIP/Postal Code
518118
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Xiaojian Jia, PhD
Phone
+86 138 2379 7115
Email
94205638@qq.com
First Name & Middle Initial & Last Name & Degree
Qi Wang, PhD
Phone
+8613688819667
Email
16981017@qq.com

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
not decided

Learn more about this trial

Clinical Study of Ligustrazine in Treating Alcohol Addiction

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