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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01544621
Other study ID # A3051150
Secondary ID
Status Completed
Phase N/A
First received February 29, 2012
Last updated May 20, 2013
Start date November 2011
Est. completion date May 2013

Study information

Verified date May 2013
Source Pfizer
Contact n/a
Is FDA regulated No
Health authority Unites States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

Real life smoking cessation rates after 24 weeks non-intervention design. Approximately 40 General Practice (GP) centers with 800 smokers will participate.


Description:

Active smokers who wish to quit seen at in primary care practices


Recruitment information / eligibility

Status Completed
Enrollment 544
Est. completion date May 2013
Est. primary completion date May 2013
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Smoking males or females aged 18 years or older.

- Subjects being motivated for and willing to quit smoking.

- Ability to read and understand Danish.

Exclusion Criteria:

- Not smoking.

- Aged below 18 years.

- Lack of motivation and willingness to quit smoking.

- Do not read and understand Danish.

- Is not willing to cooperate with the clinic staff.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms


Intervention

Other:
Smoking cessation
Smoking cessation

Locations

Country Name City State
n/a

Sponsors (2)

Lead Sponsor Collaborator
Pfizer Technical University of Denmark (DTU)

Outcome

Type Measure Description Time frame Safety issue
Primary Share of participants not smoking six months after the quit date. Intention-to-treat calculation, where participants lost to follow-up are included in as continued smokers 6 months No
Secondary Share of participants not smoking six months after the quit date Per protocol calculation (participants lost to follow-up are excluded in the calculation of the quit rate) 6 months No
Secondary Share of participants at six months not smoking the last 14 days Intention-to-treat calculation, where participants lost to follow-up are included in as continued smokers 6 months No
Secondary Share of participants at six months not smoking the last 14 days Per protocol calculation (participants lost to follow-up are excluded in the calculation of the quit rate) 6 months No
Secondary Share of participants not smoking at the last visit at the GP Intention-to-treat calculation, where participants lost to follow-up are included in as continued smokers 6 months No
Secondary Share of participants not smoking at the last visit at the GP. Per protocol calculation (participants lost to follow-up are excluded in the calculation of the quit rate) 6 months No
Secondary Share of participants still smoking at six months with a reduction in the use of tobacco and the resulting reduction in smoking Intention-to-treat calculation, where participants lost to follow-up are included in as continued 6 months No
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