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Effect of Nicotine Pouches on The Underlying Normal Electrocardiogram

Effect of Nicotine Pouches on The Underlying Normal Electrocardiogram A Double-Blinded, Placebo-Controlled Cross-over Study Exploring the Dose-Response Effects of Nicotine Pouches on Heart Rate and the Electrocardiogram ACRONYM: The NICOTUNE Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07057440
Acronym
NICOTUNE
Enrollment
20
Registered
2025-07-09
Start date
2025-06-27
Completion date
2025-10-31
Last updated
2025-12-11

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

Conditions

ECG, Heart Rate, Symptoms, Vital Sign Monitoring

Brief summary

Nicotine pouches (NPs) are increasingly being used by children, adolescents, and adults, and are often presented as a less harmful alternative to, for example, smoking. The ability to use these products discreetly (unlike smoking) makes them an attractive option for individuals who wish to avoid the stigma that smokers may sometimes experience. Nicotine is a well-known addictive substance that affects many organ systems, including the heart and circulatory system. The amount of nicotine in NPs varies greatly, but the pouches can contain large amounts of nicotine compared to the content of a single cigarette. While many studies have previously examined the effects of smoking and other nicotine products on the heart and circulatory system, specific data on the effects of NPs on these same systems are rather limited. In light of the above, the investigators have planned a study to investigate whether NPs affect the circulatory system and heart rate, assessed through electrocardiography (ECG) and vital signs (i.e., pulse, blood pressure, respiratory rate, and more). The investigators hypothesis is that the nicotine content in NPs leads to notable changes in the aforementioned measurements and could therefore potentially be associated with an increased health risk.

Interventions

OTHERHigh-dose Nicotine Pouch

A High Dose Nicotine Pouch are placed and held in the oral cavity (between the gum and lip) for 20 minutes, as per standard use instructions. After 20 minutes pouches are removed from the oral cavity and disposed.

OTHERLow Dose Nicotine Pouch

A Low Dose Nicotine Pouch are placed and held in the oral cavity (between the gum and lip) for 20 minutes, as per standard use instructions. After 20 minutes pouches are removed from the oral cavity and disposed.

OTHERPlacebo Pouch

A Placebo Pouch are placed and held in the oral cavity (between the gum and lip) for 20 minutes, as per standard use instructions. After 20 minutes pouches are removed from the oral cavity and disposed.

Sponsors

Ekim Seven
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Adults aged 18-70 years. * Regular (defined as daily) or occasional (generally defined as nondaily) nicotine users (e.g., cigarettes, vaping, or nicotine pouches). * Willingness to abstain from nicotine, caffeine (including caffeine containing energy drinks), and alcohol for 6 hours prior to the session

Exclusion criteria

* History of cardiovascular conditions. * Medications affecting cardiac conduction or autonomic function (e.g., antiarrhythmic drugs). * Pregnancy or breastfeeding. * Current illness or infection. * History of substance abuse.

Design outcomes

Primary

MeasureTime frameDescription
Heart rate10 and 20 minutes (just before disposal) after the placement of the nicotine pouch in the oral cavityChanges in HR (beats/minute) obtained from an ECG recorded 20 minutes after nicotine pouch administration compared to the baseline ECG.

Secondary

MeasureTime frameDescription
ECG parameters10 and 20 minutes (just before disposal) after the placement of the nicotine pouch in the oral cavityChanges in various ECG parameters from baseline: • PR interval (msec) • QRS duration (msec) • QT interval (corrected, QTc) (msec) • HRV (msec)
ST-T segment changes10 and 20 minutes (just before disposal) after the placement of the nicotine pouch in the oral cavityST-T segment changes, e.g., depression/elevation/inversion (mm) from baseline
Arrhythmias10 and 20 minutes (just before disposal) after the placement of the nicotine pouch in the oral cavityAny arrhythmias e.g., ectopic beats (yes/no, numerical) detected on the ECG compared with baseline ECG

Other

MeasureTime frameDescription
Blood pressure10 and 20 minutes (just before disposal) after the placement of the nicotine pouch in the oral cavityChanges in Blood pressure (mmHg)
Self-reported symptoms10 and 20 minutes (just before disposal) after the placement of the nicotine pouch in the oral cavitySubjective symptoms self-reported by the participants during the intervention using VAS-questionnaire of 10 known nicotine effect/symptoms (nausea, dizziness, lightheadedness, nervousness, sweatiness, headache, excessive salivation, heart pounding, confusion, and weakness).
Respiratory rate10 and 20 minutes (just before disposal) after the placement of the nicotine pouch in the oral cavityChanges in Respiratory rate (breaths per minute)
Oxygen saturation10 and 20 minutes (just before disposal) after the placement of the nicotine pouch in the oral cavityChanges in Oxygen saturation (percentage/%)
Body temperature10 and 20 minutes (just before disposal) after the placement of the nicotine pouch in the oral cavityChanges in Body temperature (degree Celsius)

Countries

Denmark

Outcome results

None listed

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