CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 52 enrolled
Drug / intervention
Nicotine patch +1 moredrug
Likely dose
Not stated in 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/NCT03847155
NCT03847155N/ACompleted

Prevention of Nicotine Abstinence in Critically Ill Patients After Major Surgery

University Hospital Ostrava·interventional·Posted Feb 20, 2019·Updated Feb 9, 2021

In Brief

A clinical study evaluating Nicotine patch and Placebo patch for Nicotine Dependence. Completed, enrolled 52 participants across 1 site.

Detailed Summary

The primary objective of this study is to determine whether the application of transdermal nicotine patches in critically ill patients after major surgery with nicotine abstinence condition is associated with a lower incidence of delirium.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCzechia
Collaborators--

Timeline

N/ACompletedFinished
20162017201820192020202120222023202420252026
First PostedFeb 20, 2019
Enrollment StartSep 23, 2015
Primary CompletionJan 31, 2021
Study CompletionFeb 8, 2021
TodayJul 2, 2026
Enrollment to primary: 5.4 yearsPosted 7.4 years ago

Interventions

Nicotine patchdrug

The patients will receive a nicotine patch for the period of a maximum of 7 days.

Placebo patchother

The patients will receive a placebo patch for the period of a maximum of 7 days.