A Phase 2 interventional study of Bupropion SR and placebo in Smoking Cessation and Pregnancy, sponsored by Watching Over Mothers & Babies Foundation. Completed at 1 site in United States. Open to female participants aged 18 Years to 45 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2013-06-11.
Sponsored by Watching Over Mothers & Babies Foundation · Phase 2, Interventional, and Treatment
The purpose of this study is to determine whether bupropion SR increases cessation and/or smoking reduction among pregnant smokers.
Primary Objective:
To evaluate the efficacy of a pharmacologic agent (bupropion SR) to achieve higher rates of smoking cessation and greater reduction in smoking during pregnancy
Secondary Objective:
To evaluate the safety of using a pharmacologic agent (bupropion SR) for smoking cessation in pregnancy.
Hypotheses to be tested:
Few studies have offered pregnant women pharmacologic assistance with their tobacco addiction for the purpose of achieving smoking cessation in pregnancy. In view of the evidence from the non-pregnant population, pharmacologic assistance with either nicotine replacement therapy or bupropion is essential to significant cessation and reduction programs. This pilot study is designed to generate sufficient preliminary data to support future grant applications to state and/or federal funding agencies for adequate funding to conduct a properly powered randomized clinical trial. This pilot study will provide useful information for future sample size calculations and give some indication as to the rate of adverse reactions and safety profile of bupropion taken during pregnancy.
Cigarette smoking is associated with various complications of pregnancy., Likewise, infants and children of women who smoke during pregnancy are at greater risk for a myriad of physical and developmental problems. Women who participate in the study and receive the intervention may benefit if they reduce or stop their tobacco use. Decreased cigarette smoking by pregnant subjects enrolled in this study may lead to a reduction in complications of pregnancy and health problems of infants and children that are attributable to smoking.
The standard therapy for pregnant women is to receive some directive counseling from their clinician. Occasionally, patients will even be referred to community organizations to reinforce the office counseling. The evidence suggests that there is limited value to behavioral counseling alone and that most clinicians are not properly trained and that those who are, do not have the time to adequately counsel patients. There are no smoking cessation programs currently available in the Tucson community that offer pharmacologic assistance in combination with counseling to pregnant women. Individual clinicians do prescribe pharmacologic aids for their patients on a case by case basis.
Smoking cessation counseling is evidence based. However, as the investigators have previously indicated it is rarely conveyed to patients because of inadequate training and time. There is currently no support within obstetrical healthcare funding to subsidize the cost of this service.
This is the only study on the registry with Watching Over Mothers & Babies Foundation as lead sponsor.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Study medication (150 mg bupropion SR) daily for 14 days. Women still smoking at 2-weeks \& 4-weeks were encouraged to increase their medication to two times per day (150 mg bid). Women received smoking cessation counseling at baseline, 2, 4, 6, and 8 weeks.
Drug: Bupropion SR · Behavioral: smoking cessation counseling
Study medication (placebo) daily for 14 days. Women still smoking at 2-weeks \& 4-weeks were encouraged to increase their medication to two times per day. Women received smoking cessation counseling at baseline, 2, 4, 6, and 8 weeks.
Drug: placebo · Behavioral: smoking cessation counseling
Comparison of bupropion SR or placebo + smoking cessation counseling
Also known as: Wellbutrin SR, Zyban SR
biologically verified smoking cessation or reduction
change in smoking from study enrollment to end of treatment (8 weeks) and at delivery
Time frame: 8 weeks and delivery
adverse events reported during pregnancy
Time frame: 8 weeks and delivery
self reported smoking cessation or reduction
change in self reported smoking from study enrollment to end of treatment (8 weeks) and at delivery
Time frame: 8 weeks and delivery
depression
change in depression (measured by the Edinburgh postnatal depression scale) between study enrollment and end of treatment (8 weeks)
Time frame: 8 weeks and delivery
This study is completed, as verified in Jun 2013. You cannot join it, but the record below documents what was studied.
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