Last updated: 11/07/2018 20:03:27
An open-label, multicentre study with general practitioners to assess efficacy and safety of Bupropion SR (2x150mg per day) as an aid to smoking cessation in patients who were previously treated with Bupropion SR or NRT
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: An open-label, multicentre study with general practitioners to assess efficacy and safety of Bupropion SR (2x150mg per day) as an aid to smoking cessation in patients who were previously treated with Bupropion SR or NRT
Trial description: An open-label, multicentre study with general practitioners to assess efficacy and safety of Bupropion SR (2x150mg per day) as an aid to smoking cessation in patients who were previously treated with Bupropion SR or NRT
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Bergmann L, Warncke W, and Herschel M. Bupropion SR for weaning from smoking in relapsed smokers: results of an open multicentre trial in Germany. Pneumologie 2004; 58: 140-146.
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
Not applicable
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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