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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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.
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.
1,028 studies on the registry are indexed under Tobacco Use Disorder; 128 are open to participants now.
Browse Tobacco Use Disorder studies →4 of the 42 studies testing Nicotine Patch in Tobacco Use Disorder are open now, in 4 countries. Recruiting first, the newest first:
Henan Provincial People's Hospital · Sites in China
Ages 18–75 · Men only
University of Oklahoma · Sites in United States
Ages 21–60 · Healthy volunteers
Jasper A. Smits · Sites in United States
Ages 18+ · Healthy volunteers
University of Southern California · Sites in Uganda, Zambia
Ages 18+ · Healthy volunteers
By country, each count listing its studies:
Nicotine Patch: first FDA approval 1991 (NICODERM CQ). What it is approved for, and how studies give it, is on its page →
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 →This tab as a report to print or save as PDF → With an account.
42 studies; the count open now beside each. This study's row is marked.
A study in two phases is counted once above. Listed by phase, each with its combined phases: Phase 1 4 · Phase 2 9 · Phase 3 8 · Phase 4 14
First in 1999; this study’s year is marked. 3 started in 2018.
By drug class, each counting the studies that test any of its medicines:
This study's enrollment of 94 is close to the median of 90 across 893 interventional studies indexed under Tobacco Use Disorder.
Median enrollment 135 across the 42 interventional studies. Of the 35 that completed or were terminated, 21 (60%) have results posted.
This tab as a report to print or save as PDF → With an account.
5 of 42 have an industry lead sponsor. The 10 most frequent:
Duke University is the lead sponsor of 2,063 studies on the registry; 272 are open to participants now.
Of its 204 completed or terminated interventional studies of FDA-regulated products, 167 (82%) have results posted.
26 studies in Tobacco Use Disorder by Duke University: 2 open now, 2 under way, none of them phase 3. Of 21 finished, 13 (62%) have results posted.
Among the 26 studies in Tobacco Use Disorder by Duke University, this one is the 9th largest by enrollment of the 25 interventional ones that give a count, is one of 4 that started in 2018, is one of 6 in phase 2, and was the 22nd registered.
Duke University’s Tobacco Use Disorder studies by the year they started, since 2007.
3 of the studies testing Nicotine Patch in Tobacco Use Disorder that are under way reach primary completion within a year, 1 of them phase 3. Phase 3 first, then by date:
| Study | Primary completion |
|---|---|
| NCT04176172Phase 3Abramson Cancer Center at Penn MedicineOptimizing Tobacco Use Treatment for PLWHA | 2026-11-30 |
| NCT07250230Henan Provincial People's HospitalEffect of Perioperative High-dose Transdermal Nicotine Patch on Pain Sensitivity Among Male Abstinent Tobacco Smokers Undergoing Thoracic Surgery: A Randomized Controlled Pilot Study | 2026-12-31 |
| NCT05587361University of OklahomaBeta-Adrenergic Modulation of Drug Cue Reactivity | 2027-03-31 |
Add all 3 to your calendar (.ics) → With an account.
Among the 42 studies testing Nicotine Patch in Tobacco Use Disorder, from their registry updates:
Among Duke University’s 26 in Tobacco Use Disorder:
Nothing recorded among them since 2026-09-25.
This tab as a report to print or save as PDF → With an account.
This study plans to investigate whether using electronic cigarettes (e-cigarettes) or skin patches containing nicotine affects switching from smoking conventional combustible (burning) cigarettes.
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.
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.
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:
Exclusion Criteria:
Use (within the past 30 days) of:
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.
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.
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.
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.
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 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 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.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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.
Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.
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
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
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
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
Participants will wear the nicotine patch daily while switching from cigarette use to use of e-cigarettes for eight weeks.
Also known as: NicoDerm
Participants will wear the placebo patch daily while switching from cigarette use to use of e-cigarettes for eight weeks.
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
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
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
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
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
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
| Milestone | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches |
|---|---|---|---|---|
| Started | 37 | 33 | 11 | 13 |
| Completed | 26 | 19 | 7 | 10 |
| Not completed | 11 | 14 | 4 | 3 |
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).
| Parts per million (ppm) | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches |
|---|---|---|---|---|
| Expired Air Carbon Monoxide (CO) to Assess Recent Smoking | 18.3 ± 16.2 | 22.9 ± 12.6 | 21.3 ± 25.7 | 25.6 ± 16.6 |
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).
| cigarettes smoked per day | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches |
|---|---|---|---|---|
| Cigarette Use, Assessed by Self-report in Daily Dairies | 9.2 ± 7.7 | 9.9 ± 9.0 | 10.3 ± 12.3 | 9.3 ± 6.9 |
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).
| e-cigarette pods per day | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches |
|---|---|---|---|---|
| E-cigarette Use, Assessed by Self-report in Daily Dairies | 2.5 ± 2.6 | 2.0 ± 2.5 | 3.5 ± 3.6 | 2.4 ± 2.1 |
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.
No measurements were reported for this outcome.
Collected over 8 weeks. Non-serious events are listed at a 5% frequency threshold.
| Group | Deaths | Serious | Other |
|---|---|---|---|
| Nicotine E-cigs + Nicotine Patches | 0/37 (0%) | 2/37 (5.4%) | 21/37 (56.8%) |
| Non-nicotine E-cigs + Nicotine Patches | 0/33 (0%) | 3/33 (9.1%) | 15/33 (45.5%) |
| Nicotine E-cigs + Placebo Patches | 0/11 (0%) | 1/11 (9.1%) | 4/11 (36.4%) |
| Non-nicotine E-cigs + Placebo Patches | 0/13 (0%) | 0/13 (0%) | 4/13 (30.8%) |
| Event | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches |
|---|---|---|---|---|
| Infected renal stoneRenal and urinary disorders | 0/37 | 0/33 | 1/11 | 0/13 |
| Streptococcal PneumoniaRespiratory, thoracic and mediastinal disorders | 0/37 | 1/33 | 0/11 | 0/13 |
| Auditory HallucinationsPsychiatric disorders | 0/37 | 1/33 | 0/11 | 0/13 |
| Hypertensive CrisisVascular disorders | 0/37 | 1/33 | 0/11 | 0/13 |
| Knee SurgerySurgical and medical procedures | 1/37 | 0/33 | 0/11 | 0/13 |
| COPD ExacerbationRespiratory, thoracic and mediastinal disorders | 1/37 | 0/33 | 0/11 | 0/13 |
| Event | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches |
|---|---|---|---|---|
| Vivid DreamsGeneral disorders | 7/37 | 6/33 | 3/11 | 1/13 |
| ItchinessSkin and subcutaneous tissue disorders | 8/37 | 3/33 | 1/11 | 1/13 |
| Rapid Heart BeatCardiac disorders | 0/37 | 0/33 | 2/11 | 0/13 |
| ConstipationGastrointestinal disorders | 0/37 | 0/33 | 2/11 | 0/13 |
| HeadacheNervous system disorders | 2/37 | 0/33 | 1/11 | 0/13 |
| InsomniaGeneral disorders | 0/37 | 3/33 | 0/11 | 1/13 |
| Dry MouthGeneral disorders | 2/37 | 0/33 | 1/11 | 0/13 |
| NauseaGastrointestinal disorders | 0/37 | 0/33 | 1/11 | 1/13 |
| VomitingGastrointestinal disorders | 0/37 | 0/33 | 1/11 | 0/13 |
| IrritabilityPsychiatric disorders | 2/37 | 2/33 | 1/11 | 0/13 |
| Age, Continuous(years) | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches | Total |
|---|---|---|---|---|---|
| Mean | 49.1 ± 9.4 | 46.0 ± 8.7 | 46.3 ± 12.5 | 45.4 ± 8.7 | 47.2 ± 10.3 |
| Sex: Female, Male(Participants) | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches | Total |
|---|---|---|---|---|---|
| Female | 25 | 17 | 6 | 8 | 56 |
| Male | 12 | 16 | 5 | 5 | 38 |
| Ethnicity (NIH/OMB)(Participants) | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches | Total |
|---|---|---|---|---|---|
| Hispanic or Latino | 0 | 0 | 0 | 0 | 0 |
| Not Hispanic or Latino | 37 | 33 | 11 | 13 | 94 |
| Unknown or Not Reported | 0 | 0 | 0 | 0 | 0 |
| Race (NIH/OMB)(Participants) | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches | Total |
|---|---|---|---|---|---|
| American Indian or Alaska Native | 0 | 1 | 0 | 0 | 1 |
| Asian | 1 | 0 | 0 | 0 | 1 |
| Native Hawaiian or Other Pacific Islander | 0 | 0 | 0 | 0 | 0 |
| Black or African American | 9 | 7 | 5 | 7 | 28 |
| White | 25 | 23 | 6 | 6 | 60 |
| More than one race | 1 | 1 | 0 | 0 | 2 |
| Unknown or Not Reported | 1 | 1 | 0 | 0 | 2 |
| Region of Enrollment(Participants) | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches | Total |
|---|---|---|---|---|---|
| United States | 37 | 33 | 11 | 13 | 94 |
| Baseline expired air carbon monoxide level(Parts per million (ppm)) | Nicotine E-cigs + Nicotine Patches | Non-nicotine E-cigs + Nicotine Patches | Nicotine E-cigs + Placebo Patches | Non-nicotine E-cigs + Placebo Patches | Total |
|---|---|---|---|---|---|
| Mean | 30.2 ± 14.3 | 27.7 ± 14.0 | 27.2 ± 13.4 | 28.5 ± 10.7 | 28.7 ± 13.5 |
PDFs hosted by the registry, ClinicalTrials.gov.
Plan to share: No
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.
This study is completed, as verified in Jan 2023. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
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Studies of the drug tested here: Nicotine Patch