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CompletedNCT01875172Updated Jun 11, 2013

Bupropion for Smoking Cessation in Pregnancy

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

Phase
Phase 2
Study type
Interventional
Enrollment
135
Allocation
Randomized
Ages
18 Years to 45 Years
Sex
Female
01

Study summary

The purpose of this study is to determine whether bupropion SR increases cessation and/or smoking reduction among pregnant smokers.

Read the detailed description

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:

  1. Bupropion SR combined with smoking cessation counseling during pregnancy will increase smoking cessation, compared to smoking cessation counseling combined with placebo, or standard of care.
  2. Bupropion SR combined with smoking cessation counseling during pregnancy will produce greater reduction in smoking in patients unable to quit, as compared to smoking cessation counseling combined with placebo, or standard of care.
  3. Bupropion SR combined with smoking cessation counseling during pregnancy will improve perinatal outcomes (by decreasing preterm birth, preterm premature rupture of membranes, antenatal bleeding, low birth weight, intrauterine growth restriction and increasing maternal weight gain), as compared to smoking cessation counseling combined with placebo, or standard of care.
  4. Bupropion SR combined with smoking cessation counseling during pregnancy will increase the rate of smoking cessation without increasing the number of adverse events reported by women, as compared to smoking cessation counseling combined with placebo, or standard of care.

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.

02

Conditions studied

  • Smoking Cessation
  • Pregnancy

Keywords

  • bupropion SR
  • randomized controlled trial
  • pregnancy
03

In context

Lead sponsor

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.

04

Who can participate

Ages eligible
18 Years to 45 Years
Sexes eligible
Female
Accepts healthy volunteers
Yes

Inclusion criteria

  • Smoked at least one puff in the past 7 days
  • Confirmed viable gestation

Exclusion criteria

Exclusion Criteria:

  • All patients found to have a non-viable fetus or major congenital anomaly
  • History of seizure disorder
  • Family history of seizure disorder
  • History of severe head trauma
  • History of anorexia nervosa or bulimia
  • Current use of nicotine-replacement therapy
  • Unstable medical or psychiatric condition
  • Current use of an monoamine oxidase inhibitor or bupropion hydrochloride products
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
135 participants (actual)

Study arms

  • Experimental
    Bupropion SR

    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

  • Placebo comparator
    Placebo

    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

Interventions

  • DrugBupropion SR

    Comparison of bupropion SR or placebo + smoking cessation counseling

    Also known as: Wellbutrin SR, Zyban SR

  • Drugplacebo
  • Behavioralsmoking cessation counseling
06

What researchers measure

Primary outcomes

  1. 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

Secondary outcomes

  1. adverse events reported during pregnancy

    Time frame: 8 weeks and delivery

  2. 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

Other outcomes

  1. 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

07

Study locations

1 site
  • Watching over Mothers and Babies Foundation
    Tucson, Arizona 85712, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 11, 2013, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT01875172
Lead sponsor
Watching Over Mothers & Babies Foundation
Collaborators
University of Arizona
Responsible party
Hugh Miller (Medical Director, Watching Over Mothers & Babies Foundation) — Principal investigator
First posted
Jun 11, 2013
Start date
Oct 2001
Primary completion
Jan 2004
Completion
Jan 2004
Last update
Jun 11, 2013

Study contacts

Hugh S Miller, MD
principal investigator · Watching Over Mothers and Babies Foundation

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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