Repetitive Transcranial Magnetic Stimulation in Patients With Opioid Use Disorders

Heroin Dependence Clinical Trial

Official title:

The Effects of Repetitive Transcranial Magnetic Stimulation in Patients With Opioid Use Disorders: Analysis of Clinical Outcomes, Functional Magnetic Resonance Imaging, Biomarkers, and Neuropsychological Tests

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT03229642
• Other study ID #: B-BR-105-094
• Status: Recruiting
• Phase: N/A
• Start date: August 1, 2017
• Est. completion date: December 31, 2022

Study information

• Verified date: September 2020
• Source: National Cheng-Kung University Hospital
• Contact: Tzu-Yun Wang
• Phone: +886-6-2353535
• Email: tzuyun0105[@]hotmail.com
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Opioid use disorder (OUD) is prevalent and causes substantial health and social burdens. Although evidence have showed the effectiveness of opioid agonist maintenance therapy in OUD, high drop-out rate and the requirement of continuing use of opioid agonists are the major problems. Therefore, to develop novel treatment for OUD is important.

Repetitive transcranial magnetic stimulation (rTMS) is a noninvasive method of brain stimulation used to treat a variety of neuropsychiatric disorders. Recent studies showed that there may be potential therapeutic effects in rTMS for addictive disorder, including reducing craving and substance use severity. The underlying mechanisms of rTMS in treating addictions may involve increased dopamine function in corticomesolimbic brain circuits and modulation of neural activity in brain circuits that relevant to addiction. However, the treatment results of rTMS in OUD were lacked, and the analysis in functional brain imaging study, neuropsychological tests and other potential biomarkers under rTMS treatment were limited, too.

Thus, the investigators will conduct the add-on double-blinded, sham-controlled study rTMS treatment in 40-60 patients with OUD under methadone maintenance therapy. Patients will be allocated to active and sham rTMS in a 1 : 1 ratio, and participants will receive rTMS on the left dorsolateral prefrontal cortex (DLPFC) (15 Hz frequency, 4 seconds per train, inter-train interval of 26 seconds, 40 trains per session, total 11 sessions in 4 weeks). The treatment response, urine drug tests, craving scales and side effects to evaluate the therapeutic effects of rTMS will be examined. Neuropsychological assessments, functional magnetic resonance imaging (fMRI) and tests for potential biomarkers of immune parameters will also be measured during 12-weeks follow up. The study results will provide the important data in whether rTMS add-on methadone maintenance therapy is able to 1) reduce heroin use; 2) reduce craving for heroin; 3) be an effective treatment for OUD, and 4) be associated with improvement in fMRI, biological markers and psychological tests.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: December 31, 2022
• Est. primary completion date: December 31, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 20 Years to 65 Years

Eligibility

Inclusion Criteria:

1. Signed informed consent by patient or legal representative.

2. Male or female patient aged ?20 and ?65 years.

3. A diagnosis of OUD according to DSM criteria made by a specialist in psychiatry.

4. Patient or a reliable caregiver can be expected to ensure acceptable compliance and visit attendance for the duration of the study.

Exclusion Criteria:

1. Women of childbearing potential, not using adequate contraception as per investigator judgment or not willing to comply with contraception for the duration of the study.

2. Females who are pregnant or lactation.

3. Current evidence of an uncontrolled and/or clinically significant medical condition, e.g.,cardiac, hepatic and renal failure that would compromise patient safety or preclude study participation.

4. History of seizure or epilepsy.

5. History of neurological diseases or traumatic brain injury.

6. Suicidal attempts or risks during screen or study period.

7. Presence of devices, e.g. pace-makers, cochlear prosthesis, neuro-stimulators, magnetic cochlear prosthesis, intraocular metallic fragments.

8. Patient has received electroconvulsive therapy (ECT) within 4 weeks prior to the first intervention of the double-blinded treatment.

Related Conditions & MeSH terms

• Heroin Dependence
• Transcranial Magnetic Stimulation

Intervention

Device:
• Active rTMS
The stimulator device was a Magstim super rapid magnetic stimulator (Magstim Company, Ltd., Wales, United Kingdom) with 4 booster modules equipped with a 70-mm air-cooled figure-eight-shaped coil. We performed rTMS on the left dorsolateral prefrontal cortex (DLPFC).The TMS parameters were as follows: 15Hz frequency, pulse intensity 100% of the rMT, 60 pulses per train, inter train pause of 26 sec, 40 stimulation trains, and 2400 total pulses for a total duration of 20 min. The patients received one rTMS session per day during the first five days of treatment, and then twice a week for the following three weeks, for a total of 11 rTMS sessions. The sham group was administered rTMS with the same parameters, but using a figure-of-eight sham coil.
• Sham rTMS
The stimulator device was a Magstim super rapid magnetic stimulator (Magstim Company, Ltd., Wales, United Kingdom) with 4 booster modules equipped with a 70-mm air-cooled figure-eight-shaped coil. We performed rTMS on the left dorsolateral prefrontal cortex (DLPFC).The TMS parameters were as follows: 15Hz frequency, pulse intensity 100% of the rMT, 60 pulses per train, inter train pause of 26 sec, 40 stimulation trains, and 2400 total pulses for a total duration of 20 min. The patients received one rTMS session per day during the first five days of treatment, and then twice a week for the following three weeks, for a total of 11 rTMS sessions. The sham group was administered rTMS with the same parameters, but using a figure-of-eight sham coil.

Locations

Country	Name	City	State
Taiwan	National Cheng Kung University Hospital	Tainan

Sponsors (2)

Lead Sponsor	Collaborator
National Cheng-Kung University Hospital	Ministry of Science and Technology, Taiwan

Country where clinical trial is conducted

Taiwan, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The treatment retention rate	To compare the treatment retention rate between the active and sham rTMS groups from baseline to endpoint (12 weeks).	12 weeks
Primary	The treatment attendance rate	To compare the treatment attendance rate between the active and sham rTMS groups from baseline to endpoint (12 weeks).	12 weeks
Primary	Urinary assessment	Urinary morphine examinations will be measured at every visit. The rate of positive urinary morphine tests will be compared between active and sham rTMS groups in 12 weeks of follow up.	12 weeks
Secondary	fMRI	The fMRI scan will be done at initial screen and at week 5 (after rTMS treatment) with resting-state fMRI and task activation fMRI with an IGT.	5 weeks
Secondary	Immunological markers	Twenty milliliters of blood will be drawn from each participant. Plasma will be isolated from the whole blood after it has been centrifuged at 3000 g for 15 min at 4?, and the will be immediately stored at -80?. Cytokine and BDNF levels will be quantified using an antibody pair assay system (Flexia; BioSource Intl., Camarillo, CA). Sample processing and data analysis will be done according to the manufacturer's instructions.; The immunological parameters that we intend to analyze will include TNF-a, CRP, TGF-ß1, IL-8, Il-10 and BDNF. The immunological markers will be measured from baseline to endpoint (week 12) in each patient group.	12 weeks
Secondary	Wechsler Memory Scale - third edition(WMS-III)	WMS-III will be tested at initial screen and at the end of study (week 12) and compared between the active and sham rTMS groups.	12 weeks
Secondary	Wisconsin Card Sorting Test(WCST)	WCST will be tested at initial screen and at the end of study (week 12) and compared between the active and sham rTMS groups.	12 weeks
Secondary	Continuous performance tests(CPT)	CPT will be tested at initial screen and at the end of study (week 12) and compared between the active and sham rTMS groups.	12 weeks
Secondary	Side effect checklist	To compare the side effect profiles using side effect checklist between the active and sham rTMS groups from baseline to endpoint (12 weeks).	12 weeks
Secondary	Assessment of craving	To compare the severity of craving between the active and sham rTMS groups from baseline to endpoint (12 weeks).	12 weeks
Secondary	17-item Hamilton Depression Rating Scale (HDRS)	To compare the mood symptoms between the active and sham rTMS groups from baseline to endpoint (12 weeks).	12 weeks
Secondary	World Health Organization's Quality of Life Assessment-Brief of Taiwan (WHOQOL-BREF TW)	To compare the life quality (using WHOQOL-BREF TW) between the active and sham rTMS groups from baseline to endpoint (12 weeks).	12 weeks
Secondary	Family APGAR index	To compare the level of family support (using family APGAR index) between the active and sham rTMS groups from baseline to endpoint (12 weeks).	12 weeks
Secondary	The Opiate Treatment Index (OTI)	To compare the OTI tween the active and sham rTMS groups from baseline to endpoint (12 weeks).	12 weeks
Secondary	Clinical Global Impressions (CGI)	To compare the CGI tween the active and sham rTMS groups from baseline to endpoint (12 weeks).	12 weeks
Secondary	Barratt Impulsiveness Scale(BIS)	To compare the BIS tween the active and sham rTMS groups from baseline to endpoint (12 weeks).	12 weeks