Clinical Trials Directory

Trials / Completed

CompletedNCT02350335

Transdermal Nicotine Replacement in Smokers With Acute Aneurysmal Subarachnoid Hemorrhage

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
200 (actual)
Sponsor
Oslo University Hospital · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

All patients with acute aneurysmal hemorrhage are treated in accordance with our institutional protocol. After securing of the aneurysm, some smokers with acute aneurysmal hemorrhage are randomly assigned to transdermal nicotine replacement (NRT). The short- and long-term effect of NRT will be studied comparing non-smokers, smokers without NRT and smokers with NRT.

Detailed description

Various aspects of the study: * Study cerebral circulation with transcranial Doppler ultrasonography (TCD) prior to and after NRT. * Study cardiac output and peripheral vessel resistance minimally invasive (LiDCO) prior to and after NRT in patients that already have established LiDCO. * Monitor intracranial pressure prior to and after NRT in patients that have established an intracranial pressure sensor. * Register the frequency of cerebral vasospasm and complications in non-smokers, smokers without NRT, and smokers with NRT. * Register the use of opioids, opioidanesthetics, propofol og psycholeptics in non-smokers, smokers without NRT, and smokers with NRT.

Conditions

Interventions

TypeNameDescription
DRUGNicotine (transdermal)Application of transdermal nicotine replacement in smokers with acute aneurysmal hemorrhage

Timeline

Start date
2011-01-01
Primary completion
2015-12-01
Completion
2015-12-01
First posted
2015-01-29
Last updated
2016-04-12

Locations

1 site across 1 country: Norway

Source: ClinicalTrials.gov record NCT02350335. Inclusion in this directory is not an endorsement.