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NCT06554873 · ClinicalTrials.gov registry record · Phase 3

Adaptive Use of Nicotine Substitution to Maintain Smoking Reduction/Abstinence in Nicotine Responders

A Phase 3 study, sponsored by Rose Research Center.

Completed
Registry status
Phase 3
Development phase
150
Enrollment target

NCT06554873 is a Phase 3 study that has completed, run by Rose Research Center. The registered enrollment target is 150 participants.

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The verdict

NCT06554873, a Phase 3 study, has completed, sponsored by Rose Research Center.

COMPLETED
Registry status
Phase 3
Development phase
150 participants
Enrollment target

Study Summary

To determine whether smokers who initially respond (within 2 weeks) to nicotine products (including nicotine replacement therapy, e-cigarettes, nicotine pouches) by reducing their smoking by ≥50% can be successfully maintained on use of these noncombustible nicotine alternatives to cigarettes for 6 months, and whether this results in sustained smoking reduction/abstinence.

Interventions

  • DRUG Nicoderm
  • DRUG Nicorette 4Mg Chewing Gum
  • DRUG Nicorette Lozenge Product
  • OTHER NJOY e-cigarette
  • OTHER on!

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2024-08-29
Est. Completion 2025-12-09
Phase Phase 3

Sponsor

Rose Research Center

11 total trials

What the Registry Record Tells You About NCT06554873

The ClinicalTrials.gov registry entry for NCT06554873 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Rose Research Center, which has 11 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 5 interventions - of which Nicoderm is the first listed.

NCT06554873 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT06554873 about?

NCT06554873 is a clinical study titled "Adaptive Use of Nicotine Substitution to Maintain Smoking Reduction/Abstinence in Nicotine Responders". To determine whether smokers who initially respond (within 2 weeks) to nicotine products (including nicotine replacement therapy, e-cigarettes, nicotine pouches) by reducing their smoking by ≥50% can be successfully maintained on use of these noncombustible nicotine alternatives to cigarettes for 6 ...

What is the current status of trial NCT06554873?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 150 participants. The study started on 2024-08-29. Estimated completion is 2025-12-09.

What interventions are being tested in trial NCT06554873?

The interventions under investigation include: Nicoderm (DRUG), Nicorette 4Mg Chewing Gum (DRUG), Nicorette Lozenge Product (DRUG), NJOY e-cigarette (OTHER), on! (OTHER).

Who is sponsoring clinical trial NCT06554873?

This trial is sponsored by Rose Research Center, which has 11 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.