Fentanyl DependenceNCT05469217
The Effects of Fentanyl Abuse on Executive Function and Related Brain Activity
An observational study of Fentanyl Dependence, run by Ariel University.
Trial summary
There is a widespread abuse of prescription opioids and a dramatic increase in the availability of illicit opioids. These have created the "opioid epidemic" which is one of the most severe public health crisis in US History. Read more about this study
- Who is it for?
- Ages 18 to 50 yearsHealthy volunteers can take part
- Conditions the study is for
- Fentanyl Dependence
- What is being tested?
- fMRI brain imaging
- How many people
- 30 participants
- Where
- No sites listed yet
- Study dates
- Sep 2022to Sep 2025
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 to 50 years
- All sexes
- Healthy volunteers accepted
- Adult
Study population: 15 patients diagnosed with Fentanyl dependence will be recruited from treatment centers and 15 healthy control participants will be recruited from the general public
Inclusion Criteria: patients with Fentanyl dependence who have used the drug over the past year - Exclusion Criteria: Neurological impairment, Infectious diseases such as HIV/AIDS, pregnant women, underage, cocaine or alcohol abuse
Healthy control participants from the general public Exclusion Criteria: Neurological impairment, Infectious diseases such as HIV/AIDS, pregnant women, underage, cocaine or alcohol abuse
-
Trial locations and contacts
No sites are listed yet.
About this study
There is a widespread abuse of prescription opioids and a dramatic increase in the availability of illicit opioids. These have created the "opioid epidemic" which is one of the most severe public health crisis in US History. Fentanyl, a synthetic opioid that is 50 to 100 times more potent than morphine, is a schedule II prescription drug used to treat severe pain. It is also a drug of abuse. Fentanyl is more likely to cause an overdose than is heroin because of its greater potency. In addition, it has a shorter half-life than most other opioids, causing the high to fade more quickly, requiring opioid drug abusers to inject more frequently, and increasing the risk of overdose. There is an increasing use of Fentanyl in Israel, and one of the treatment centers has reported that on average each month over the last year 10 patients that have used fentanyl were admitted. We propose to investigate executive function using established tasks such as the N-back and Go No Go tasks as well as structural brain imaging of gray matter volume and white matter tracts in 15 fentanyl abuse patients that will be compared with 15 healthy control participants.
Read the detailed description
There is a widespread abuse of prescription opioids and a dramatic increase in the availability of illicit opioids. These have created the "opioid epidemic" which is one of the most severe public health crisis in US History (Skolnik, 2018; Volkow and Blanco, 2021). The magnitude of this epidemic is alarming. About 4% of the adult US population misuses prescription opioids, and in 2015, more than 33,000 deaths were attributable to overdose with licit and illicit opioids including Fentanyl (Skolnik, 2018). The number has increased in 2019 to 49,860 and in 2020 to over 93,000 deaths (Mattson et al., 2021; Lancet, 2021). The magnitude of the phenomenon is huge since there are over 125 million Americans suffering from either acute or chronic pain, and there is an urgent need for a long-term solution for controlling and ultimately eradicating this epidemic (Skolnik, 2018; France et al., 2021).
During the Covid-19 epidemic among individuals tested, there was an increase by 35% for non-prescribed fentanyl and 44% for heroin (Niles et al., (2021). Positive tests for non-prescribed fentanyl increased significantly among patients positive for other drugs: by 89% for specimens positive for amphetamines; 48% for benzodiazepines; 34% for cocaine; and 39% for opiates (Niles et al., 2021).
Fentanyl, a synthetic opioid that is 50 to 100 times more potent than morphine, is a schedule II prescription drug used to treat severe pain. It is also a drug of abuse. However, evidence from drug seizures by the US Drug Enforcement Agency indicates that fentanyl-related harm, overdose, and deaths in the United States are usually the result of illegally made fentanyl, sold through illicit drug markets for its euphoric effect. Fentanyl is more likely to cause an overdose than is heroin because of its greater potency. In addition, it has a shorter half-life than most other opioids, causing the high to fade more quickly, requiring opioid drug abusers to inject more frequently, and increasing the risk of overdose (Niles et al., 2021). The low production costs of fentanyl and its potency (50- fold compared to heroin) make it an attractive option to mix with heroin and illicit manufactured prescription opioids (Frank et al., 2017).
There is an increasing use of Fentanyl in Israel, and one of the treatment centers called "Haderech" in Ilabun has reported that on average each month over the last year 10 patients that have used fentanyl were admitted.
Currently, there are few studies that have investigated the effects of chronic long-term effects of opiate use on cognitive function and the brain. Steenbergen et al., (2019) have suggested that the mu-opioid system can influence higher-level cognitive function via modulation of evaluation, motivation, and control circuits dense in mu-opioid receptors, including the orbitofrontal cortex, basal ganglia, amygdala, anterior cingulate cortex, and the prefrontal cortex. They have proposed that opioids influence decision making and cognitive control by increasing the subjective value of reward and reducing aversive arousal (Steenbergn et al., 2019).
Initial research utilizing whole-brain neuroimaging techniques has identified structural differences in gray matter in opioid-dependent individuals although the results have been inconsistent. Wollman et al., (2017) have reported a meta-analysis of neuroimaging findings from 12 studies comparing opioid-dependent individuals to drug-naïve controls. Using Anisotropic Effect-Size Seed-Based d Mapping (AES-SDM) they have found that the fronto-temporal region, bilaterally, was the primary site of gray matter deficits associated with opioid use. Moderator analysis revealed that length of opioid use was negatively associated with gray matter in the left cerebellar vermis and the right Rolandic operculum, including the insula. Meta-regression revealed no remaining significant areas of gray matter reductions, except in the precuneus, following longer abstinence from opioids. They have concluded that Opioid-dependent individuals had significantly less gray matter in the frontal-cerebellar system that might be responsible for impulsivity, compulsive behaviors, and affective disturbances and the frontal-insular system that might account more for the cognitive and decision-making impairments.
To the best of our knowledge, there are no studies that have evaluated executive function impairment and gray matter and white matter structural changes as a result of fentanyl abuse. We propose to investigate executive function using established tasks such as the N-back task and structural brain imaging of gray matter volume and white matter tracts in 15 fentanyl abuse patients that will be compared with 15 healthy control participants. Patients will be recruited after treatment in the Israeli Ministry of Health treatment centers in Israel. The cognitive tasks and questionnaires evaluating drug abuse, anxiety and depression will be done by research assistants from the Dept. of Psychology and Behavioral science in Ariel University under responsibility of the co-principal investigator Prof. Aviv Weinstein. Structural fMRI imaging will be done in the dept. of diagnostic imaging in Tel Hashomer hospital under responsibility of the co-principal investigator Dr. Abigail Livny. We anticipate that this will be a pioneer study that may have major implications for our understanding of the long-term consequences of fentanyl abuse.
References France CP, Ahern GP, Averick S, Disney A, Enright HA, Esmaeli-Azad B, Federico A, Gerak LR, Husbands SM, Kolber B, Lau EY, Lao V, Maguire DR, Malfatti MA, Martinez G, Mayer BP, Pravetoni M, Sahibzada N, Skolnick P, Snyder EY, Tomycz N, Valdez CA, Zapf J. Countermeasures for Preventing and Treating Opioid Overdose. Clin Pharmacol Ther. 2021; 109(3):578-590. doi: 10.1002/cpt.2098. Epub 2020 Nov 29.
Frank RG, Pollack HA. Addressing the Fentanyl Threat to Public Health. The New England Journal of Medicine 2017; 376(7): 605-607.
The Lancet. A time of crisis for the opioid epidemic in the USA. Lancet. 2021; 24;398 (10297):277. doi: 10.1016/S0140-6736(21)01653-6.
Mattson CL, Tanz LJ, Quinn K, Kariisa M, Patel P, Davis NL. Trends and Geographic Patterns in Drug and Synthetic Opioid Overdose Deaths - United States, 2013-2019. MMWR Morb Mortal Wkly Rep 2021; 70:202-207. DOI: http://dx.doi.org/10.15585/mmwr.mm7006a4external icon Niles JK, Gudin J, Radcliff J, Kaufman HW. The Opioid Epidemic Within the COVID-19 Pandemic: Drug Testing in 2020. Popul Health Manag. 2021; 24(S1):S43-S51. doi: 10.1089/pop.2020.0230. Epub 2020 Oct 8.
Skolnick P. The Opioid Epidemic: Crisis and Solutions. Annu Rev Pharmacol Toxicol. 2018; 6;58:143-159. doi: 10.1146/annurev-pharmtox-010617-052534. Epub 2017 Oct 2.
van Steenbergen, H., Eikemo, M. \& Leknes, S. The role of the opioid system in decision making and cognitive control: A review. Cogn Affect Behav Neurosci 19, 435-458 (2019). https://doi.org/10.3758/s13415-019-00710-6 Volkow ND, Blanco C. The changing opioid crisis: development, challenges and opportunities. Mol Psychiatry. 2021; 26(1):218-233. doi: 10.1038/s41380-020-0661-4. Epub 2020 Feb 4.
Wollman SC, Alhassoon OM, Hall MG, Stern MJ, Connors EJ, Kimmel CL, Allen KE, Stephan RA, Radua J. Gray matter abnormalities in opioid-dependent patients: A neuroimaging meta-analysis. Am J Drug Alcohol Abuse. 2017; 43(5):505-517. doi: 10.1080/00952990.2016.1245312. Epub 2016 Nov 3. PMID: 27808568.
- Conditions
- Fentanyl Dependence
- Being tested
- fMRI brain imaging
- Keywords
- Fentanyl, gray matter, white matter, VBM, N-Back
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
fMRI brain imagingOther
Structural MRI of gray and white matter, functional MRI during performance of the N-back task
| Study group | Role | What they receive |
|---|---|---|
| Fentanyl dependent patients | 15 participants who were treated for fentanyl dependence in treatment centers in Israel Receives: Other: fMRI brain imaging | |
| Control participants | Healthy control participants from the general public Receives: Other: fMRI brain imaging |
What is being measured
The primary outcome is the main question the study is designed to answer.
Gray matter volume in fMRI
Measures of gray matter volume in MRI
Measured: 2 years
White matter volume in fMRI
Measures of white matter tracts in DTI in MRI
Measured: 2 years
Executive function
Measures of brain activity on the N-Back task in fMRI
Measured: 2 years
Secondary outcomes (1)
N-back
Measures of performance on the N-Back task in fMRI
Measured: 2 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted21 Jul 2022
- Study startSep 2022 (estimated)
- Primary completionSep 2024 (estimated)
- Study completionSep 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Fentanyl DependenceStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Enrolment
- 30 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Ariel University
- Sponsor type
- University, hospital or other
- Collaborators
- Sheba Medical Center
- Responsible party
- Sponsor
- Investigators
- Galia Zarfati, MD, Principal investigator, Sheba Tel Hashomer Medical Center
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT05469217
- Sponsor's protocol ID
- SMC-9459-22
- Status last verified
- Jul 2022
- First submitted
- 20 Jul 2022
- Last updated
- 21 Jul 2022
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 21 Jul 2022. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Effects of Fentanyl Abuse on Executive Function and Related Brain Activity
- ClinicalTrials.gov ID
- NCT05469217
- Acronym / sponsor ID
- SMC-9459-22
- Conditions
- Fentanyl Dependence
- Keywords
- Fentanyl, gray matter, white matter, VBM, N-Back
- Study type
- Observational
- Recruitment status
- Unknown status
- Enrolment
- 30 participants (estimated)
- Lead sponsor
- Ariel UniversityUniversity, hospital or other
- Collaborators
- Sheba Medical Center
- Study start
- Sep 2022 (estimated)
- Primary completion
- Sep 2024 (estimated)
- Study completion
- Sep 2025 (estimated)
- First posted
- 21 Jul 2022 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
There is a widespread abuse of prescription opioids and a dramatic increase in the availability of illicit opioids. These have created the "opioid epidemic" which is one of the most severe public health crisis in US History. Fentanyl, a synthetic opioid that is 50 to 100 times more potent than morphine, is a schedule II prescription drug used to treat severe pain. It is also a drug of abuse. Fentanyl is more likely to cause an overdose than is heroin because of its greater potency. In addition, it has a shorter half-life than most other opioids, causing the high to fade more quickly, requiring opioid drug abusers to inject more frequently, and increasing the risk of overdose. There is an increasing use of Fentanyl in Israel, and one of the treatment centers has reported that on average each month over the last year 10 patients that have used fentanyl were admitted. We propose to investigate executive function using established tasks such as the N-back and Go No Go tasks as well as structural brain imaging of gray matter volume and white matter tracts in 15 fentanyl abuse patients that will be compared with 15 healthy control participants.
Detailed description
There is a widespread abuse of prescription opioids and a dramatic increase in the availability of illicit opioids. These have created the "opioid epidemic" which is one of the most severe public health crisis in US History (Skolnik, 2018; Volkow and Blanco, 2021). The magnitude of this epidemic is alarming. About 4% of the adult US population misuses prescription opioids, and in 2015, more than 33,000 deaths were attributable to overdose with licit and illicit opioids including Fentanyl (Skolnik, 2018). The number has increased in 2019 to 49,860 and in 2020 to over 93,000 deaths (Mattson et al., 2021; Lancet, 2021). The magnitude of the phenomenon is huge since there are over 125 million Americans suffering from either acute or chronic pain, and there is an urgent need for a long-term solution for controlling and ultimately eradicating this epidemic (Skolnik, 2018; France et al., 2021).
During the Covid-19 epidemic among individuals tested, there was an increase by 35% for non-prescribed fentanyl and 44% for heroin (Niles et al., (2021). Positive tests for non-prescribed fentanyl increased significantly among patients positive for other drugs: by 89% for specimens positive for amphetamines; 48% for benzodiazepines; 34% for cocaine; and 39% for opiates (Niles et al., 2021).
Fentanyl, a synthetic opioid that is 50 to 100 times more potent than morphine, is a schedule II prescription drug used to treat severe pain. It is also a drug of abuse. However, evidence from drug seizures by the US Drug Enforcement Agency indicates that fentanyl-related harm, overdose, and deaths in the United States are usually the result of illegally made fentanyl, sold through illicit drug markets for its euphoric effect. Fentanyl is more likely to cause an overdose than is heroin because of its greater potency. In addition, it has a shorter half-life than most other opioids, causing the high to fade more quickly, requiring opioid drug abusers to inject more frequently, and increasing the risk of overdose (Niles et al., 2021). The low production costs of fentanyl and its potency (50- fold compared to heroin) make it an attractive option to mix with heroin and illicit manufactured prescription opioids (Frank et al., 2017).
There is an increasing use of Fentanyl in Israel, and one of the treatment centers called "Haderech" in Ilabun has reported that on average each month over the last year 10 patients that have used fentanyl were admitted.
Currently, there are few studies that have investigated the effects of chronic long-term effects of opiate use on cognitive function and the brain. Steenbergen et al., (2019) have suggested that the mu-opioid system can influence higher-level cognitive function via modulation of evaluation, motivation, and control circuits dense in mu-opioid receptors, including the orbitofrontal cortex, basal ganglia, amygdala, anterior cingulate cortex, and the prefrontal cortex. They have proposed that opioids influence decision making and cognitive control by increasing the subjective value of reward and reducing aversive arousal (Steenbergn et al., 2019).
Initial research utilizing whole-brain neuroimaging techniques has identified structural differences in gray matter in opioid-dependent individuals although the results have been inconsistent. Wollman et al., (2017) have reported a meta-analysis of neuroimaging findings from 12 studies comparing opioid-dependent individuals to drug-naïve controls. Using Anisotropic Effect-Size Seed-Based d Mapping (AES-SDM) they have found that the fronto-temporal region, bilaterally, was the primary site of gray matter deficits associated with opioid use. Moderator analysis revealed that length of opioid use was negatively associated with gray matter in the left cerebellar vermis and the right Rolandic operculum, including the insula. Meta-regression revealed no remaining significant areas of gray matter reductions, except in the precuneus, following longer abstinence from opioids. They have concluded that Opioid-dependent individuals had significantly less gray matter in the frontal-cerebellar system that might be responsible for impulsivity, compulsive behaviors, and affective disturbances and the frontal-insular system that might account more for the cognitive and decision-making impairments.
To the best of our knowledge, there are no studies that have evaluated executive function impairment and gray matter and white matter structural changes as a result of fentanyl abuse. We propose to investigate executive function using established tasks such as the N-back task and structural brain imaging of gray matter volume and white matter tracts in 15 fentanyl abuse patients that will be compared with 15 healthy control participants. Patients will be recruited after treatment in the Israeli Ministry of Health treatment centers in Israel. The cognitive tasks and questionnaires evaluating drug abuse, anxiety and depression will be done by research assistants from the Dept. of Psychology and Behavioral science in Ariel University under responsibility of the co-principal investigator Prof. Aviv Weinstein. Structural fMRI imaging will be done in the dept. of diagnostic imaging in Tel Hashomer hospital under responsibility of the co-principal investigator Dr. Abigail Livny. We anticipate that this will be a pioneer study that may have major implications for our understanding of the long-term consequences of fentanyl abuse.
References France CP, Ahern GP, Averick S, Disney A, Enright HA, Esmaeli-Azad B, Federico A, Gerak LR, Husbands SM, Kolber B, Lau EY, Lao V, Maguire DR, Malfatti MA, Martinez G, Mayer BP, Pravetoni M, Sahibzada N, Skolnick P, Snyder EY, Tomycz N, Valdez CA, Zapf J. Countermeasures for Preventing and Treating Opioid Overdose. Clin Pharmacol Ther. 2021; 109(3):578-590. doi: 10.1002/cpt.2098. Epub 2020 Nov 29.
Frank RG, Pollack HA. Addressing the Fentanyl Threat to Public Health. The New England Journal of Medicine 2017; 376(7): 605-607.
The Lancet. A time of crisis for the opioid epidemic in the USA. Lancet. 2021; 24;398 (10297):277. doi: 10.1016/S0140-6736(21)01653-6.
Mattson CL, Tanz LJ, Quinn K, Kariisa M, Patel P, Davis NL. Trends and Geographic Patterns in Drug and Synthetic Opioid Overdose Deaths - United States, 2013-2019. MMWR Morb Mortal Wkly Rep 2021; 70:202-207. DOI: http://dx.doi.org/10.15585/mmwr.mm7006a4external icon Niles JK, Gudin J, Radcliff J, Kaufman HW. The Opioid Epidemic Within the COVID-19 Pandemic: Drug Testing in 2020. Popul Health Manag. 2021; 24(S1):S43-S51. doi: 10.1089/pop.2020.0230. Epub 2020 Oct 8.
Skolnick P. The Opioid Epidemic: Crisis and Solutions. Annu Rev Pharmacol Toxicol. 2018; 6;58:143-159. doi: 10.1146/annurev-pharmtox-010617-052534. Epub 2017 Oct 2.
van Steenbergen, H., Eikemo, M. \& Leknes, S. The role of the opioid system in decision making and cognitive control: A review. Cogn Affect Behav Neurosci 19, 435-458 (2019). https://doi.org/10.3758/s13415-019-00710-6 Volkow ND, Blanco C. The changing opioid crisis: development, challenges and opportunities. Mol Psychiatry. 2021; 26(1):218-233. doi: 10.1038/s41380-020-0661-4. Epub 2020 Feb 4.
Wollman SC, Alhassoon OM, Hall MG, Stern MJ, Connors EJ, Kimmel CL, Allen KE, Stephan RA, Radua J. Gray matter abnormalities in opioid-dependent patients: A neuroimaging meta-analysis. Am J Drug Alcohol Abuse. 2017; 43(5):505-517. doi: 10.1080/00952990.2016.1245312. Epub 2016 Nov 3. PMID: 27808568.
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Fentanyl dependent patients | – | Other: fMRI brain imaging15 participants who were treated for fentanyl dependence in treatment centers in Israel |
| Control participants | – | Other: fMRI brain imagingHealthy control participants from the general public |
Who may qualify
- Ages
- 18 to 50 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult
- Study population
- 15 patients diagnosed with Fentanyl dependence will be recruited from treatment centers and 15 healthy control participants will be recruited from the general public
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| fMRI brain imagingStructural MRI of gray and white matter, functional MRI during performance of the N-back task | Other | Control participants, Fentanyl dependent patients |
Primary outcome
Gray matter volume in fMRI
Time frame: 2 years
Measures of gray matter volume in MRI
White matter volume in fMRI
Time frame: 2 years
Measures of white matter tracts in DTI in MRI
Executive function
Time frame: 2 years
Measures of brain activity on the N-Back task in fMRI
1 secondary outcome
N-back
Time frame: 2 years
Results and safety
Results are not available in the source record.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 21 Jul 2022.
- Individual participant dataSharing planned: No
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Galia Zarfati, MD principal investigator
Sheba Tel Hashomer Medical Center
Questions about this trial
What is this clinical trial studying?
An observational study of Fentanyl Dependence, run by Ariel University.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: status not confirmed, as of the sponsor's last update on 21 Jul 2022. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
Results are not available in the source record.
How can a doctor refer a patient or contact the research team?
Contact Aviv M Weinstein, Ph.D (+972524307610, avivweinstein@yahoo.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Gray matter volume in fMRI (time frame: 2 years). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 21 Jul 2022.