CI

At a glance

ClinicalIndex Comparison Record
Phase 4Completed· 23 enrolled
Drug / intervention
Nicotine Replacement Productdrug
Likely dose
Nicotine Replacement Product 14mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT06051474
NCT06051474Phase 4Completed

Treating Nicotine Addiction in Caregivers of Children at American Family Children's Hospital

University of Wisconsin, Madison·interventional·Posted Sep 25, 2023·Updated Apr 16, 2026

In Brief

A Phase 4 clinical trial evaluating Nicotine Replacement Product for Smoking and Smoking Cessation. Completed, enrolled 23 participants across 1 site.

Detailed Summary

The purpose of this research study is to 1) see if a smoking cessation program is something that caregivers will use while their child is hospitalized, 2) see if caregivers think this program is something we should institute across the hospital, and 3) see if this program can help caregivers reduce their smoking. Participants will: * Complete a survey regarding smoking behavior and thoughts about quitting; * Undergo a 20-minute counseling session; and, * Use nicotine patches and mini-lozenges for 2 weeks

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 4CompletedFinished
202420252026
First PostedSep 25, 2023
Enrollment StartMar 5, 2024
Primary CompletionApr 18, 2025
TodayJul 2, 2026
Enrollment to primary: 1.1 yearsPosted 2.8 years ago

Interventions

Nicotine Replacement Productdrug

Adults will receive a 2-week supply of nicotine patches to place on skin (14mg or 21mg; dosing depending on tobacco use per package insert) and oral nicotine mini-lozenges (2mg, 4mg, dosing depending on tobacco use per package insert). All participants will also receive a single smoking cessation counseling session with a physician. Surveys will be completed pre-intervention, within 24 hours of hospital discharge, and 2-weeks after hospital discharge.