Transdermal Nicotine Replacement in Smokers With Acute Aneurysmal Subarachnoid Hemorrhage (NRT-SAH)
Aneurysmal Subarachnoid Hemorrhage
About this trial
This is an interventional treatment trial for Aneurysmal Subarachnoid Hemorrhage focused on measuring aneurysm, nicotine replacement therapy, cerebral vasospasm, outcome
Eligibility Criteria
Inclusion Criteria:
- aneurysmal subarachnoid hemorrhage after securing of the aneurysm and surviving the first 2 weeks.
Exclusion Criteria:
- manifest cerebral vasospasm at arrival at our department (i.e. before securing of the aneurysm)
Sites / Locations
- Oslo University Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Active Comparator
No Intervention
No Intervention
NRT
no NRT
non-smokers
Active smokers with acute aneurysmal hemorrhage randomly assigned to transdermal nicotine replacement after securing of the aneurysm. Patient management for all patients is according to the institutional treatment guidelines and independent of group assignment. The dose is dependent on smoke consumption prior to the ictus. Nicorette 7 mg/day for smokers smoking 1-10 cigarettes /day Nicorette 14mg/day for smokers smoking 11-19 cigarettes/day Nicorette 21 mg/day for smokers smoking 20 or more cigarettes daily
Active smokers with acute aneurysmal hemorrhage that were assigned to not receive transdermal nicotine replacement.
Non-smokers with acute aneurysmal hemorrhage. Non-smokers do not receive transdermal nicotine replacement. This group is to be compared to the group of active smokers receiving transdermal nicotine replacement and to the group of active smokers not receiving transdermal nicotine replacement.