Attention Deficit Hyperactivity Disorder (ADHD) Smoking Cessation Study

Duke University

Status

Completed

Conditions

Nicotine Dependence

Attention Deficit Hyperactivity Disorder

Treatments

Drug: Transdermal Nicotine Patch

Drug: Lis-dexamphetamine (Vyvanse)

Drug: Placebo

Study type

Interventional

Funder types

Other

Industry

Identifiers

NCT00736255

SPD489-607 (Other Grant/Funding Number)

Pro00001248

Details and patient eligibility

About

The overall goal of the present project is to investigate whether lisdexamphetamine (LDX; Vyvanse) is an effective adjunct to nicotine replacement therapy (NRT) to promote smoking cessation in patients with comorbid Attention Deficit Hyperactivity Disorder (ADHD) and nicotine dependence. The investigators hypothesized initially that smokers with ADHD who are optimized to a dose of LDX prior to quitting smoking and who remain on this dose of medication after quitting will remain abstinent longer than patients who are treated with placebo before and after quitting.However due to recent key issues that have arisen showing that initiation of stimulant treatment while subjects are actively smoking may facilitate increased smoking, and given that the study was still in the very early stage of study execution, the investigators revised the study design to use an empirically validated pretreatment approach with NRT and to initiate LDX treatment on the first post quit date in order to reduce the withdrawal symptoms that accompany smoking cessation. The overall rationale for this revised study design remains similar to the original.

Full description

This will be a 2-group, parallel, placebo-controlled, double blind study. Regular, nicotine dependent individuals with ADHD will receive NRT pretreatment for 2 weeks prior to an identified quit date.At the quit date, subjects will be randomized into one of two groups.

The first group will begin treatment for 1 week with LDX 30 mg and then will be titrated up to 50mg and 70mg if tolerated. Subjects will continue on the highest tolerated dose until the 4th week. Concurrently subjects will receive transdermal NRT, 21 mg at week one, 14 mg at week 2 and 7 mg at weeks 3 and 4.
The second group will receive matching placebo and transdermal NRT after the quit date.

Participants will attend a total of 16 visits over a period of 7-11 weeks. The primary outcome measure for this study will be the proportion of individuals in each group who report 4 weeks continuous smoking abstinence verified by both Carbon Monoxide (CO) levels and salivary cotinine, measured at Visit 5. It is hypothesized that the group co-treated with LDX will have a significantly higher proportion of individuals who remain abstinent across the 4 weeks measured every other day.

Inclusion Criteria:

Aged 18-50 years
Meet DSM-IV criteria (Diagnostic and Statistical manual of mental Disorders Version 4) for ADHD, any subtype; assessed using the Conners Adult ADHD Interview for DSM (CAADID)
Meet DSM-IV criteria for nicotine dependence as verified by afternoon expired CO levels of >15 parts per million (PPM) and self-report of smoking >10 cigarettes/day
Free from major medical problems and deemed healthy by the study physician
Not currently receiving medication for ADHD or other psychiatric disorders. If a patient is screened as is currently receiving medication for ADHD, they may be enrolled, provided they washout of their current medication for an appropriate length of time.
No contraindications for treatment with either LDX or transdermal nicotine

Exclusion Criteria:

DSM-IV Axis I or Axis II disorders that require additional pharmacological treatment or otherwise would interfere with participation in the present study
History of known cardiovascular disease, clinically significant hypertension, or other cardiovascular risk factors which, in the opinion of the study physician, would contraindicate treatment
BMI (Body Mass Index) > 35

Enrollment

32 patients

Sex

All

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Attention Deficit Hyperactivity Disorder(ADHD) diagnosis
smokes at least > 10 cigarettes per day
no major medical problems
no contraindications to treatment with either LDX or transdermal nicotine

Exclusion criteria

other psychiatric conditions that require medication
history of cardiovascular disease, clinically significant hypertension
Body Mass index (BMI) > 35

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

32 participants in 2 patient groups, including a placebo group

Vyvanse and transdermal nicotine patch

Experimental group

Description:

The first group will receive LDX/SPD489 titrated up to 70 mg qd for 4 weeks after the identified quit date. Subjects will continue to receive NRT 21 mg at week 1 post quit date, then 14mg at week 2 post quit date and 7 at weeks 3 and 4 post quit date.

Treatment:

Drug: Lis-dexamphetamine (Vyvanse)

Drug: Transdermal Nicotine Patch

Placebo and transdermal nicotine patch

Placebo Comparator group

Description:

The second group will receive matching placebo and NRT after the quit date.

Treatment:

Drug: Placebo

Drug: Transdermal Nicotine Patch