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TerminatedNCT02439944

Efficacy and Neural Correlates of Personalized Treatment With Transdermal Nicotine Replacement

Medication studyAges 19–65CanadaAddiction
The study in practice

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Who could participate?

Listed age limits: 19 years to 65 years.

Listed locations
TorontoSee all locations and recruitment
Study phase
Phase 2 / Phase 3This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.

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What to know before participating

A point to clarify

This summary does not cover all risks or eligibility requirements. What risks or changes to my care would apply to me?

Study clarity

Things to check before joining

Study start dateStarted: July 2015
Recruitment status
Terminated
Enrollment listed in the registry
18
Sponsor
Centre for Addiction and Mental Health
Sponsor type
Hospital / academic medical center
Study type
Drug
Intervention type
Drug
Study phase
Phase 2 / Phase 3This study spans more than one phase, so it may combine goals such as safety, dosing, and early effectiveness.
Locations
Canada
Age range
From 19 Years to 65 Years
Official registry ID
NCT02439944
Official title
Show the full official title

Efficacy and Neural Correlates of Personalized Treatment With Transdermal Nicotine Replacement: A Randomized, Controlled Pilot Study in Motivated Smokers Unable to Quit With Standard Dosing

Recruitment & locations

Terminated

Toronto

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FAQ

Questions about this study

Who is behind this study?

The study sponsor is Centre for Addiction and Mental Health, a hospital or academic medical center.

Does this study involve medication?

Yes. The study involves medication, including Nicotine patch and Nicotine mouthspray.

Who can participate?

Listed age limits: 19 years to 65 years.

Is this study still recruiting?

The registry lists this study as terminated.

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