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Nicotine Metabolizers and [11C]-(+)-PHNO

Influence of Nicotine Metabolism Ratio on [11C]-(+)-PHNO PET Binding in Tobacco Smokers

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02514720
Acronym
MET
Enrollment
16
Registered
2015-08-04
Start date
2015-06-30
Completion date
2017-01-31
Last updated
2018-09-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Nicotine Dependence

Brief summary

The purpose of this study is to investigate the effects of nicotine metabolism on occupancy of \[11C\]-(+)-PHNO to DA 2/3 receptors in different brain areas during periods of abstinence and smoking during an abstinence. This will be a Positron Emission Tomography (PET) study and the radiotracer \[11C\]-(+)-PHNO (11C\]-( + )-4-propyl- 3,4,4a,5,6,10b-hexahydro-2H-naphtho\[1,2-b\]\[1,4\]oxazin-9-ol) will be used.

Detailed description

The participants will undergo a PET scan after approximately 48 hours abstinence (to ensure total elimination of nicotine in both FMs and SMs) and then approximately \>5 hours later may have a second PET scan after smoking their preferred cigarette (approximately 1 hour before). It is possible that these two scans may also occur on separate days. All subjects will provide a urine sample for (1) drug toxicology, (2) pregnancy test (in females) and (3) Total Nicotine Equivalents (TNE: a measure of total consumption unaltered by rate of nicotine metabolism). There will one blood draw taken before and one after each PET scan (about 20mls in total) to measure nicotine and COT levels (to assess abstinence) as well as kinetics of nicotine delivery. Participants will be given questionnaires prior to, or during, and/or after one or both of the PET scans to determine differences between abstinence and smoking on subjective measures..

Interventions

Participants will be allowed to smoke a cigarette prior to a PET scan and be abstinent from smoking prior to the other PET scan

Sponsors

Centre for Addiction and Mental Health
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Males and females of any ethnic origin 18 years of age or older. * No previous use of medication for smoking cessation in previous month- * Non-treatment seeker * Either SMs or FMs by NMR

Exclusion criteria

* DSM-IV diagnosis of other drug dependences * Any medical condition requiring immediate investigation or treatment * Pregnancy tested by urine or lactation by self-report * Current diagnosis of any Axis I psychiatric disorder * Regular use of any therapeutic or recreational psychoactive drug use that may interfere with PET scanning * Exposure to radiation in the last 12 months exceding permissible limit for participants participating in research * Current use of medication that may interfere with \[11C\]-(+)-PHNO * Metal implants or paramagnetic objects within the body which may interfere with the MRI * Claustrophobia or a history of panic attacks * Having any clinical condition, drug sensitivity, or prior therapy which, in the investigator's opinion, makes the participant unsuitable for the study * Current use of antidepressants that may inhibit CYP2A6 or impact response to nicotine

Design outcomes

Primary

MeasureTime frameDescription
Occupancy of D2/3 receptors by [11C]-(+)-PHNO2 weeksFast and slow nicotine metabolizers will have PET scans and occupancy of dopamine receptors will be measured using a PET scanner.

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026