Deep Brain Stimulation of the Bilateral Nucleus Accumbens for Patients With Methadone Maintenance Treatment

January 7, 2020 updated by: Bomin Sun, Ruijin Hospital

Methadone maintenance treatment (MMT) is one of the main forms of treatments for opioid dependence. Despite its effectiveness and widespread use, people will experience withdrawal if daily dose is insufficient or missed, promoting reluctance to attempt detoxification. In addition, methadone is a full opioid agonist which can induce respiratory depression or sedation without ceiling level, so overdose usage can be fatal. Hence, an alternative therapy is needed to completely reduce the carving for drugs and to relieve the negative affective sate caused by withdrawal.

Deep brain stimulation (DBS) is a reasonable treatment approach for addiction. Since 2009 the first case report emerged, the nucleus accumbens (NAc) is still the only brain target to be investigated in clinical case series of DBS for alcohol and heroin addiction.

This research will mainly investigate the effectiveness and safety of NAc-DBS for patients with methadone maintenance treatment. The investigators will also explore the influence of NAc-DBS on brain activity and cognition.

Study Overview

Study Type

Interventional

Enrollment (Anticipated)

12

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Shanghai
      • Shanghai, Shanghai, China, 200025
        • Recruiting
        • Shanghai Ruijin Hospital Functional Neurosurgery

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 65 years (ADULT, OLDER_ADULT)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • MINI diagnosis of substance dependence;
  • Proficiency in Mandarin language;
  • Failure to detox more than three times;
  • Long-term methadone maintenance treatment;
  • Capacity to provide informed consent (understanding of the study purpose and methods);

Exclusion Criteria:

  • Schizophrenia(MINI diagnosis);
  • Antisocial personality disorder(MINI diagnosis);
  • Contraindications of a MRI-examination, e.g. implanted cardiac pacemaker/heart defibrillator;
  • Severe cognitive impairments(MoCA ≤ 22);
  • Enrollment in other clinical trials;
  • Stereotactic respectively neurosurgical intervention in the past;
  • Contraindications of stereotactic intervention, e.g. increased bleeding disposition, cerebrovascular diseases (e.g. arteriovenous malfunction, aneurysms, systemic vascular diseases);
  • Serious or instable organic diseases (e.g. instable coronal heart disease);
  • Tested positively for HIV;
  • Pregnancy and/or lactation;
  • Epilepsy or other severe brain trauma or neurological impairments;

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: TREATMENT
  • Allocation: NA
  • Interventional Model: SINGLE_GROUP
  • Masking: NONE

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
EXPERIMENTAL: DBS
All subjects will undergo bilateral surgical implantation of DBS system in the Nucleus Accumbens. The DBS system will be active at two days after surgery.
We plan to use the SceneRay 1242 (SceneRay, SuZhou, China) electrode with a diameter of 1.27 mm and 4 contacts. The SceneRay 1242 electrode combined with the SceneRay 1181 implantable pulse generator has the advantage of adaptive coverage area for the Ventral Capsule/Ventral Striatum, enabling simultaneous implantation in the nucleus accumbens (NAc; 2 ventral contacts) and the anterior limb of the internal capsule (ALIC; 2 dorsal contacts) with independently programmed parameters such as frequency, amplitude, and voltage; and remote and wireless programing, which allows for convenient and prompt adjustments in emergency situations. The contact length is 3.0 mm and the spacings between the ventral and dorsal contacts are 2 mm, 4 mm, and 4 mm, respectively, spanning a total length of 22.5 mm (3 + 2 + 3 + 4 + 3 + 4 + 3 mm, with 0.5 mm projecting from the electrode tip).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Changes in Methadone dose
Time Frame: Baseline (preoperative),1 month, 3 months,6 months,9 months, 12 months
The volume of daily methadone the patients used.
Baseline (preoperative),1 month, 3 months,6 months,9 months, 12 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Hamilton Depression Scale(HAMD-17)
Time Frame: Baseline(preoperative),1 month, 3 months, 6 months, 9 months, 12 months
17 items, Total scores<7: normal; 7<Total scores≤17: possible depression; 17<Total scores≤24: definite depression; Total score>24: severe depression
Baseline(preoperative),1 month, 3 months, 6 months, 9 months, 12 months
Hamilton Anxiety Scale (HAMA)
Time Frame: Baseline(preoperative),1 month, 3 months, 6 months,9 months, 12 months
14 items, Total scores<6: normal; 7<Total scores≤14: possible anxiety; 14<Total scores≤21:definite anxiety; Total score>21: severe anxiety
Baseline(preoperative),1 month, 3 months, 6 months,9 months, 12 months
Young Manic Rating Scale (YMRS)
Time Frame: Baseline(preoperative),1 month, 3 months, 6 months,9 months, 12 months
The Young Mania Rating Scale (YMRS) is one of the most frequently utilized rating scales to assess manic symptoms. The scale has 11 items and is based on the patient's subjective report of his or her clinical condition.
Baseline(preoperative),1 month, 3 months, 6 months,9 months, 12 months
Monitoring of Side Effects Scale (MOSES)
Time Frame: Baseline(preoperative),1 month, 3 months, 6 months,9 months, 12 months
To evaluate side effects. The higher score means more severity of side effects.
Baseline(preoperative),1 month, 3 months, 6 months,9 months, 12 months
Changes in Subjective Opiate Withdrawal Scale(SOWS)
Time Frame: Baseline(preoperative),1 month, 3 months, 6 months,9 months, 12 months
Subjective Opiate Withdrawal Scale is a 16-item self-reported scale assessing severity of opiate withdrawal. Each item is rated on a 5-point Likert scale, ranging form 0(not at all) to 4(extremely).
Baseline(preoperative),1 month, 3 months, 6 months,9 months, 12 months
Obsessive compulsive drug use scale(OCDUS)
Time Frame: Baseline(preoperative),1 month, 3 months, 6 months,9 months, 12 months
Obsessive compulsive drug use scale is a 13-item self-rating scale measuring opiate craving. The total score ranges from 0 to 52. The higher score indicates stronger carving.
Baseline(preoperative),1 month, 3 months, 6 months,9 months, 12 months
The MOS item short from health survey (SF-36)
Time Frame: Baseline(preoperative),1 month, 3 months,6 months,9 months, 12 months
36 items. To evaluate the quality of life and the higher score indicates better quality of life.
Baseline(preoperative),1 month, 3 months,6 months,9 months, 12 months
World Health Organization Quality of Life-BREF (WHO-BREF)
Time Frame: Baseline(preoperative),1 month, 3 months,6 months,9 months, 12 months
26 items. The higher score means the better quality of life.
Baseline(preoperative),1 month, 3 months,6 months,9 months, 12 months
Fagerstrom Test for Nicotine Dependence assessment (FTND)
Time Frame: Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
To evaluate Nicotine Dependence. The higher of scores indicates higher level of Nicotine Dependence
Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
Beck depression inventory(BDI)
Time Frame: Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
The BDI contains 21 questions, each answer scored on a scale value of 0 to 3. 0-13: minimal depression;14-19:mild depression; 20-28:moderate depression; and 29-63:severe depression. Higher total score indicate more severe depressive symptoms.
Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
Beck anxiety inventory(BAI)
Time Frame: Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
The BAI contains 21 questions, each answer scored on a scale value of 0 to 3. 0-21: mild anxiety;22-35: moderate anxiety;36-63:severe anxiety. Higher total score indicate more severe anxiety symptoms.
Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
Perceived stress scale(PSS-10)
Time Frame: Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
The PSS-10 is a classic stress assessment instrument. Each item is rated on a 5-likert scale ranging form 0(never) to 4(often). Higher score indicate more severity of stress symptom.
Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
Twenty Item Positive and Negative Affect Schedule (PANAS)
Time Frame: Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
The PANAS contains two subscales: positive and negative subscale. Each item is rated on a 5-likert scale ranging from 1(Not at all) to 5(severely, it bothered me a lot).
Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
Work and Social Adjustment Scale(WSAS)
Time Frame: Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
Self-rated scale. The maximum score of the WSAS is 40, lower scores are better.
Baseline(preoperative),1 month, 3months,6months,9 months, 12 months
Cognitive performance
Time Frame: Baseline(preoperative),6 months,12 months
Cognitive performance is measured by a series of tasks which include stop signal task, paired associated memory, spatial working memory, stocking of Cambridge, intra-extra dimensional set shift, Bart, Beads, Delay discounting task, model-based and model-free task, avoid-approach task, dot-probe task, drug rating task.
Baseline(preoperative),6 months,12 months
Brain activity
Time Frame: Baseline(preoperative), 6 months,12 months
PET(Positron Emission Tomography) or fMRI(functional Magnetic Resonance Imaging) are used in this study.
Baseline(preoperative), 6 months,12 months

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Barratt impulsiveness scale
Time Frame: Baseline(preoperative)
The Barratt Impulsiveness Scale is a questionnaire designed to assess the personality/behavioral construct of impulsiveness which is composed of 30 items describing common impulsive or non-impulsive (for reverse scored items) behaviors and preferences. It has three 2nd order facets which are attentional, motor and non-planning. Each facet has 10 items. Higher score means greater impulsivity.
Baseline(preoperative)
UPPS-P impulsive behavior scale
Time Frame: Baseline(preoperative)
The UPPS-P Impulsive Behavior Scale is a 59-item questionnaire assessing impulsive personality traits. Each item is rated on a 4-point scale ranging from 1 (agree strongly) to 4 (disagree strongly) to indicate subject's agreement with statements. This scale includes the following five subscales: negative urgency (NU), lack of premeditation (LPM), lack of perseverance (LPS), sensation seeking (SS) and positive urgency (PU). Higher score represents a greater level of impulsivity.
Baseline(preoperative)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (ACTUAL)

May 13, 2019

Primary Completion (ANTICIPATED)

June 1, 2021

Study Completion (ANTICIPATED)

June 1, 2021

Study Registration Dates

First Submitted

May 14, 2019

First Submitted That Met QC Criteria

May 14, 2019

First Posted (ACTUAL)

May 16, 2019

Study Record Updates

Last Update Posted (ACTUAL)

January 10, 2020

Last Update Submitted That Met QC Criteria

January 7, 2020

Last Verified

May 1, 2019

More Information

Terms related to this study

Other Study ID Numbers

  • 2019 NAc-DBS MMT

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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