ClinicalTrials.gg
CompletedNCT03492463ENDS-SwitchUpdated Feb 8, 2023Results posted

The Role of Nicotine Dose and Route of Delivery in Affecting Adoption of E-cigarettes and Reducing Exposure to Toxic Combustion Products

A Phase 2 interventional study of Nicotine patch and Placebo patch in Nicotine Dependence, Cigarettes, sponsored by Duke University. Completed at 1 site in United States. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2023-02-08.

Sponsored by Duke University · Phase 2, Interventional, and Basic science

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Phase
Phase 2
Study type
Interventional
Enrollment
94
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
01

Where this study stands

Counted across the records on this site · 2026-11-15

Among 42 studies testing Nicotine Patch in Tobacco Use Disorder — 4 open to participants now, 5 under way, 2 of them phase 3. Nicotine Patch · Tobacco Use Disorder.

Enrollment
29th of 42
94 · median 135
Started
2018
with 2 others
Phase 2
6 of 42
none open now
Registered
33rd of 42
by date
Lead sponsor
3 of 42
Duke University

Among the 42 studies testing Nicotine Patch in Tobacco Use Disorder, this one is the 29th largest by enrollment, is one of 3 that started in 2018, is one of 6 in phase 2, and was the 33rd registered.

Tobacco Use Disorder

1,028 studies on the registry are indexed under Tobacco Use Disorder; 128 are open to participants now.

Browse Tobacco Use Disorder studies →

Open to participants now

4 of the 42 studies testing Nicotine Patch in Tobacco Use Disorder are open now, in 4 countries. Recruiting first, the newest first:

By country, each count listing its studies:

All 4 open studies →

About Nicotine Patch

Nicotine Patch: first FDA approval 1991 (NICODERM CQ). What it is approved for, and how studies give it, is on its page →

Who these studies take

Of the 95 Tobacco Use Disorder studies recruiting now, 42 (44%) set no upper age limit and 50 (53%) stop at 75 or younger; 6 take children under 18; 37 take healthy volunteers.

This study: 18 Years to 65 Years · all sexes · no healthy volunteers.

The full table on the hub →

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Watch this landscapeDownload CSVNarrow it in search →With an account: a weekly mail of what changed among 42 studies testing Nicotine Patch in Tobacco Use Disorder, or all of them as a file.
02

Study summary

This study plans to investigate whether using electronic cigarettes (e-cigarettes) or skin patches containing nicotine affects switching from smoking conventional combustible (burning) cigarettes.

Read the detailed description

This study proposes to assess the relative role of nicotine dose and route of delivery in affecting successful switching from combustible cigarettes to e-cigarettes, as well as concomitant reductions in ad libitum cigarette smoking and exposure to harmful and potentially harmful constituents of combustion. The strategy will be to assess adoption of e-cigarette use and concomitant reduction in ad libitum smoking of subjects' usual brands of cigarettes over an 8-week period, during which they will receive nicotine or non-nicotine e-cigarettes, and nicotine skin patches. The nicotine patches will not be used as a therapeutic treatment in this study, but rather as a way to manipulate the nicotine dose, while varying the rate and route of nicotine delivery. Behavioral or "habit" aspects of e-cigarette use will be controlled for by the groups receiving non-nicotine e-cigarettes. Initially the study design included placebo patch control conditions, but due to limitations in budget and period of support, enrollment in these these arms was discontinued. All participants currently receive active nicotine patches.

03

Conditions studied

  • Nicotine Dependence, Cigarettes

Keywords

  • Nicotine addiction
  • Cigarette smoking
  • Nicotine patches
  • E-cigarettes
04

Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Smoke an average of at least 10 cigarettes per day;
  • Have smoked at least one cumulative year;
  • Have an expired air CO reading of at least 10ppm;
  • Have a body weight of > 110 lbs. (50 kg) and ≤ 300 lbs. (136 kg);
  • Are able to read and understand English;

Potential subjects of child bearing potential must agree to use acceptable during their participation in this study. Potential subjects must agree to avoid the following during their participation in this study:

  • Participation in any other nicotine-related modification strategy outside of this protocol;
  • Use of tobacco products other than cigarettes, including pipe tobacco, cigars, snuff, and chewing tobacco;
  • Use of e-cigarettes other than the ones provided during the study;
  • Use of experimental () drugs or devices;
  • Use of illegal drugs;
  • Use of exclusionary medications.

Exclusion criteria

Exclusion Criteria:

  • Seeking treatment for nicotine dependence.
  • Hypertension - systolic BP > 160 mm Hg, diastolic BP > 100 mm Hg. Individuals with a history of hypertension may be allowed to participate in the study if the study physician or medical provider determines that the condition is stable and will not jeopardize the individual's safety.
  • Hypotension (with symptoms) - systolic BP \< 90 mm Hg, diastolic BP \< 60 mm Hg.
  • Coronary heart disease with symptoms (e.g., chest pain)
  • Heart attack in the past year
  • Cardiac rhythm disorder (irregular heart rhythm with symptoms)
  • Chest pain in the last month (unless history indicates a non-cardiac source)
  • Symptomatic heart disorder such as heart failure
  • Advanced liver or kidney disease that requires medication or dialysis, paracentesis
  • Major gastrointestinal illness (e.g. Celiac disease, Crohn's dx Ulcerative Colitis)
  • Bleeding stomach ulcers in the past 30 days
  • Lung disease that requires oxygen
  • Major brain disorder (including stroke with residual deficit, brain tumor, and seizure disorder)
  • Migraine headaches that occur more frequently than once per week
  • Recent, unexplained fainting spells
  • Problems giving blood samples
  • Diabetes with insulin use or with over 7%
  • Current cancer or treatment for cancer in the past six months (except basal or squa-mous cell skin cancer)
  • , , or
  • History of Tuberculosis or recent positive purified protein derivative (PPD)
  • Other major medical condition (as determined by study physician)
  • Currently symptomatic psychiatric disease (as determined by study physician)
  • Psychosis, bipolar disorder, or psychiatric hospitalization within the past 12 months
  • Suicidal ideation (thinking about ways to commit suicide) (within the past 12 months) or a lifetime occurrence of attempted suicide;
  • Current depression - The Patient Health Questionnaire PHQ-9 for Depression will be used to screen for current (within 2 weeks) depression. Potential subjects who score >9 (or who score >0 on item #9 ("Thoughts that you would be better off dead, or of hurting yourself in some way") will be excluded from study participation, and, at the discretion of the study physician, referred to appropriate psychiatric treatment;
  • Pregnant or nursing mothers
  • Use (within the past 30 days) of:

    • Illegal drugs (or if the urine drug screen is positive for tetrahydrocannabinol (THC), Cocaine, Amphetamine, Opiates, Methamphetamines, phencyclidine (PCP), Benzodiazepines, or Barbiturates), unless recent use of prescription Opiates or Benzodiazepines were taken for management of acute symptoms (e.g., tooth extraction, recent surgery);
    • Experimental () drugs;
    • Psychiatric medications including antidepressants (selective serotonin reuptake inhibitors (SSRIs), serotonin-norepinephrine reuptake inhibitors (SNRIs), tricyclic antidepressant (TCAs), monoamine oxidase inhibitors (MAOIs), St. John's Wort), lithium, anti-psychotics or any other medications that are known to affect smoking cessation (e.g. clonidine);
    • Phentermine, triptans, tryptophan, linezolid, dextromethorphan, opiates (unless taken for management of acute symptoms), tramadol, or dopamine agonists;
    • Any agents that have documented correlation with increased incidence of valvulopathy and/or pulmonary hypertension (e.g., cyproheptadine, trazodone, nefazodone, amoxapine, tricyclic antidepressants, mirtazapine, pergolide, ergotamine, methysergide) (or anticipated use during the study);
    • Wellbutrin, bupropion, Zyban, Chantix, varenicline, nicotine patch, nicotine replacement therapy or any other smoking cessation aid;
    • Use of cigars, cigarillos, pipes, Hookah, dissolvable nicotine, snuff, chewing tobacco, or e-cigarettes
  • Concurrent use of a serotonergic agent/combination associated with severe serotonin syndrome (within the past 30 days)
  • Use of cigars, cigarillos, pipes, Hookah, dissolvable nicotine, snuff, chewing tobacco, or e-cigarettes within the past 30 days
  • Self-report of consuming more than 6 alcoholic drinks on 1 or more days per week
  • Significant adverse reaction to nicotine patch in the past
  • Current participation or recent participation (in the past 30 days) in another smoking study at our Center or another research facility
  • Current participation in another research study
Terms in these criteria, in plain language(6)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Contraception

Ways of preventing pregnancy. “Highly effective” methods fail less than 1% of the time a year when used correctly — for example an IUD or an implant.

Criteria usually say which methods count and how long to keep using them after the last dose, sometimes for male participants too. Some studies accept a partner’s vasectomy if it was confirmed successful and that person is the participant’s only sexual partner.

Investigational drug or device

A drug or device being studied in a clinical trial.

It may be new, or already approved and being studied for another use, dose or form. Criteria often leave out people who took part in another study of one within a recent period, commonly 30 days or five half-lives.

HbA1c

A blood test of average blood sugar over the past two to three months, given as a percentage or in mmol/mol. 6.5% (48 mmol/mol) or more is the usual threshold for diabetes, normally confirmed by a second test.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

05

Study design

Phase
Phase 2
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Care provider)
Enrollment
94 participants (actual)

Study arms

  • Active comparator
    Nicotine e-cigs + Nicotine patches

    Participants will receive e-cigarettes containing nicotine and nicotine patches (21mg/24hr) and will be asked to switch from cigarette use to use of the study e-cigarettes for eight weeks.

    Drug: Nicotine patch · Other: E-cigarettes

  • Active comparator
    Non-nicotine e-cigs + Nicotine patches

    Participants will receive e-cigarettes not containing nicotine and nicotine patches (21mg/24hr) and will be asked to switch from cigarette use to use of the study e-cigarettes for eight weeks.

    Drug: Nicotine patch · Other: Non-nicotine e-cigarettes

  • Active comparator
    Nicotine e-cigs + Placebo patches

    Participants will receive e-cigarettes containing nicotine and placebo patches (21mg/24hr) and will be asked to switch from cigarette use to use of the study e-cigarettes for eight weeks.

    Other: Placebo patch · Other: E-cigarettes

  • Placebo comparator
    Non-nicotine e-cigs + Placebo patches

    Participants will receive e-cigarettes not containing nicotine and placebo patches (21mg/24hr) and will be asked to switch from cigarette use to use of the study e-cigarettes for eight weeks.

    Other: Placebo patch · Other: Non-nicotine e-cigarettes

Interventions

  • Participants will wear the nicotine patch daily while switching from cigarette use to use of e-cigarettes for eight weeks.

    Also known as: NicoDerm

  • OtherPlacebo patch

    Participants will wear the placebo patch daily while switching from cigarette use to use of e-cigarettes for eight weeks.

  • OtherE-cigarettes

    Participants will use e-cigarettes containing nicotine while switching from cigarette use to use of e-cigarettes for eight weeks.

    Also known as: Electronic Nicotine Delivery System (ENDS), e-cigs, electronic cigarettes

  • OtherNon-nicotine e-cigarettes

    Participants will use e-cigarettes not containing nicotine while switching from cigarette use to use of e-cigarettes for eight weeks.

    Also known as: Electronic Nicotine Delivery System (ENDS), e-cigs, electronic cigarettes

06

What researchers measure

Primary outcomes

  1. Expired Air Carbon Monoxide (CO) to Assess Recent Smoking

    The effects of e-cigarette nicotine content and patch nicotine content on the concurrent use of conventional cigarettes will be assessed by comparing the groups on the expired air carbon monoxide (CO) measured at the end of the exposure period (Week 8).

    Time frame: Week 8

Secondary outcomes

  1. Cigarette Use, Assessed by Self-report in Daily Dairies

    The effects of e-cigarette nicotine content and patch nicotine content on the concurrent use of conventional cigarettes will be assessed by comparing the groups on self-report of cigarette consumption on daily diaries (for week 8 only, average cigarettes smoked per day).

    Time frame: Week 8

  2. E-cigarette Use, Assessed by Self-report in Daily Dairies

    The effects of e-cigarette nicotine content and patch nicotine content on the concurrent use of e-cigarettes will be assessed by comparing the groups on self-report of e-cigarette use on daily diaries (for week 8 only).

    Time frame: Week 8

  3. Total Urinary 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL)

    The effects of e-cigarette nicotine content and patch nicotine content on the concurrent use of conventional cigarettes will be assessed by comparing the groups on total urinary NNAL, a metabolite of the tobacco-specific carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), at the end of week 8.

    Time frame: Week 8

07

Results

Posted Jun 28, 2022

Participant flow

Participant flow — Overall Study
MilestoneNicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo Patches
Started37331113
Completed2619710
Not completed111443

Outcome measures

PrimaryExpired Air Carbon Monoxide (CO) to Assess Recent Smoking

The effects of e-cigarette nicotine content and patch nicotine content on the concurrent use of conventional cigarettes will be assessed by comparing the groups on the expired air carbon monoxide (CO) measured at the end of the exposure period (Week 8).

Time frame:
Week 8
Reported as:
Mean · Parts per million (ppm)
Expired Air Carbon Monoxide (CO) to Assess Recent Smoking
Parts per million (ppm)Nicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo Patches
Expired Air Carbon Monoxide (CO) to Assess Recent Smoking18.3 ± 16.222.9 ± 12.621.3 ± 25.725.6 ± 16.6
Statistical analysis
  • Nicotine E-cigs + Nicotine Patches vs Non-nicotine E-cigs + Nicotine Patches · Regression, Linear · p = 0.01
SecondaryCigarette Use, Assessed by Self-report in Daily Dairies

The effects of e-cigarette nicotine content and patch nicotine content on the concurrent use of conventional cigarettes will be assessed by comparing the groups on self-report of cigarette consumption on daily diaries (for week 8 only, average cigarettes smoked per day).

Time frame:
Week 8
Reported as:
Mean · cigarettes smoked per day
Cigarette Use, Assessed by Self-report in Daily Dairies
cigarettes smoked per dayNicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo Patches
Cigarette Use, Assessed by Self-report in Daily Dairies9.2 ± 7.79.9 ± 9.010.3 ± 12.39.3 ± 6.9
Statistical analysis
  • Nicotine E-cigs + Nicotine Patches vs Non-nicotine E-cigs + Nicotine Patches · ANOVA · p = 0.8
SecondaryE-cigarette Use, Assessed by Self-report in Daily Dairies

The effects of e-cigarette nicotine content and patch nicotine content on the concurrent use of e-cigarettes will be assessed by comparing the groups on self-report of e-cigarette use on daily diaries (for week 8 only).

Time frame:
Week 8
Reported as:
Mean · e-cigarette pods per day
E-cigarette Use, Assessed by Self-report in Daily Dairies
e-cigarette pods per dayNicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo Patches
E-cigarette Use, Assessed by Self-report in Daily Dairies2.5 ± 2.62.0 ± 2.53.5 ± 3.62.4 ± 2.1
Statistical analysis
  • Nicotine E-cigs + Nicotine Patches vs Non-nicotine E-cigs + Nicotine Patches · ANOVA · p = 0.5
SecondaryTotal Urinary 4-(Methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL)

The effects of e-cigarette nicotine content and patch nicotine content on the concurrent use of conventional cigarettes will be assessed by comparing the groups on total urinary NNAL, a metabolite of the tobacco-specific carcinogen 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK), at the end of week 8.

Time frame:
Week 8

No measurements were reported for this outcome.

Adverse events

Collected over 8 weeks. Non-serious events are listed at a 5% frequency threshold.

Adverse event summary by group
GroupDeathsSeriousOther
Nicotine E-cigs + Nicotine Patches0/37 (0%)2/37 (5.4%)21/37 (56.8%)
Non-nicotine E-cigs + Nicotine Patches0/33 (0%)3/33 (9.1%)15/33 (45.5%)
Nicotine E-cigs + Placebo Patches0/11 (0%)1/11 (9.1%)4/11 (36.4%)
Non-nicotine E-cigs + Placebo Patches0/13 (0%)0/13 (0%)4/13 (30.8%)
Most frequent serious events
Most frequent serious events
EventNicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo Patches
Infected renal stoneRenal and urinary disorders0/370/331/110/13
Streptococcal PneumoniaRespiratory, thoracic and mediastinal disorders0/371/330/110/13
Auditory HallucinationsPsychiatric disorders0/371/330/110/13
Hypertensive CrisisVascular disorders0/371/330/110/13
Knee SurgerySurgical and medical procedures1/370/330/110/13
COPD ExacerbationRespiratory, thoracic and mediastinal disorders1/370/330/110/13
Most frequent other events
Showing 10 of 17
Most frequent other events
EventNicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo Patches
Vivid DreamsGeneral disorders7/376/333/111/13
ItchinessSkin and subcutaneous tissue disorders8/373/331/111/13
Rapid Heart BeatCardiac disorders0/370/332/110/13
ConstipationGastrointestinal disorders0/370/332/110/13
HeadacheNervous system disorders2/370/331/110/13
InsomniaGeneral disorders0/373/330/111/13
Dry MouthGeneral disorders2/370/331/110/13
NauseaGastrointestinal disorders0/370/331/111/13
VomitingGastrointestinal disorders0/370/331/110/13
IrritabilityPsychiatric disorders2/372/331/110/13

Baseline characteristics

Age, Continuous
Age, Continuous(years)Nicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo PatchesTotal
Mean49.1 ± 9.446.0 ± 8.746.3 ± 12.545.4 ± 8.747.2 ± 10.3
Sex: Female, Male
Sex: Female, Male(Participants)Nicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo PatchesTotal
Female25176856
Male12165538
Ethnicity (NIH/OMB)
Ethnicity (NIH/OMB)(Participants)Nicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo PatchesTotal
Hispanic or Latino00000
Not Hispanic or Latino3733111394
Unknown or Not Reported00000
Race (NIH/OMB)
Race (NIH/OMB)(Participants)Nicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo PatchesTotal
American Indian or Alaska Native01001
Asian10001
Native Hawaiian or Other Pacific Islander00000
Black or African American975728
White25236660
More than one race11002
Unknown or Not Reported11002
Region of Enrollment
Region of Enrollment(Participants)Nicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo PatchesTotal
United States3733111394
Baseline expired air carbon monoxide level
Baseline expired air carbon monoxide level(Parts per million (ppm))Nicotine E-cigs + Nicotine PatchesNon-nicotine E-cigs + Nicotine PatchesNicotine E-cigs + Placebo PatchesNon-nicotine E-cigs + Placebo PatchesTotal
Mean30.2 ± 14.327.7 ± 14.027.2 ± 13.428.5 ± 10.728.7 ± 13.5
08

Study locations

1 site
  • Duke Center for Smoking Cessation
    Durham, North Carolina 27705, United States
09

References and documents

Study documents

PDFs hosted by the registry, ClinicalTrials.gov.

Individual participant data

Plan to share: No

10

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Ran from Aug 2018 to primary completion in May 2021, 33 months.

Results were first posted in Jun 2022, 1 year after primary completion.

Of 37 non-industry phase 2 interventional studies under Tobacco Use Disorder, half reached primary completion within 35 months of starting (the median), counting those still running; a quarter within 19 and three quarters within 46. This study's 33 months is close to that.

Counting every sponsor, half of 41 studies reached it within 35 months; a quarter within 19 and three quarters within 43.

How these figures are worked out, and which studies are left out of them.

Registered
Apr 3, 2018
First posted
Apr 10, 2018
StartActual
Aug 6, 2018
Primary completionActual
May 31, 2021
CompletionActual
May 31, 2021
Results first posted
Jun 28, 2022
Last update
Feb 8, 2023
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Feb 8, 2023, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
11

Registry details

Key details

Study ID
NCT03492463
Lead sponsor
Duke University
Responsible party
Sponsor
First posted
Apr 10, 2018
Start date
Aug 6, 2018
Primary completion
May 31, 2021
Completion
May 31, 2021
Results posted
Jun 28, 2022
Last update
Feb 8, 2023

Study contacts

Jed E. Rose, Ph.D.
principal investigator · Duke University

Oversight

Data monitoring committee
No
FDA-regulated drug
Yes
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Jan 2023. You cannot join it, but the record below documents what was studied.

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Studies of the drug tested here: Nicotine Patch

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