Viewing Study NCT00228098



Ignite Creation Date: 2024-05-05 @ 12:02 PM
Last Modification Date: 2024-10-26 @ 9:19 AM
Study NCT ID: NCT00228098
Status: UNKNOWN
Last Update Posted: 2005-09-28
First Post: 2005-09-26

Brief Title: Smoking Cessation Intervention After Stroke or Transient Ischaemic Attack
Sponsor: Odense University Hospital
Organization: Odense University Hospital

Study Overview

Official Title: Smoking Cessation Intervention After Stroke or Transient Ischaemic Attack A Randomised Controlled Trial
Status: UNKNOWN
Status Verified Date: 2005-09
Last Known Status: RECRUITING
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Patients with stroke or transient ischemic attach should receive advise on smoking cessation It is however unknown if an intensive smoking cessation program is better than ordinary advise on smoking cessation during hospitalisation for stroke or transient ischemic attack

The aim of the study was to assess if an intensive smoking cessation program made more patients stop smoking after stroke or transient ischemic attack
Detailed Description: Patients with stroke or transient ischemic attach should receive advise on smoking cessation It is however unknown if an intensive smoking cessation program is better than ordinary advise on smoking cessation during hospitalisation for stroke or transient ischemic attack

The aim of the study was to assess if an intensive smoking cessation program made more patients stop smoking after stroke or transient ischemic attack

Patients with stroke or transient ischemic attack are admitted to the department of neurology at Odense University hospital Patient who are smokers on admission and age 76 years inhabitants in Funen County and with symptoms developed before admission will be offered participation in the study unless they have severe stroke stroke more than 3 weeks before admission other severe disease or unable to participate

Study participants will be randomised to either usual short advise on smoking cessation or an intensive smoking cessation program All participants will be followed-up for 6 months with regard to smoking habits

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None