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Smoking CessationPhase 2NCT01875172

Bupropion for Smoking Cessation in Pregnancy

A Phase 2 study testing Bupropion SR and smoking cessation counseling in people with Smoking Cessation and Pregnancy, run by Watching Over Mothers & Babies Foundation at 1 site in United States.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

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

Who is it for?
Ages 18 to 45 years, women onlyHealthy volunteers can take part
Conditions the study is for
Smoking Cessation, Pregnancy
What is being tested?
Bupropion SR and smoking cessation counseling
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
135 participants
Where
1 siteUnited States
Study dates
Oct 2001to Jan 2004
Phase
Phase 2
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 45 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

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

Who cannot join

  • 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

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Watching over Mothers and Babies Foundation

    Tucson, Arizona, 85712

Other trials in United States

About this study

Official title: Smoking Cessation in Pregnancy: A Pilot Study Comparing Counseling With and Without Sustained-Release Bupropion

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.

Being tested
Bupropion SR, placebo, smoking cessation counseling
Keywords
bupropion SR, randomized controlled trial, pregnancy
Medical subject headings
Smoking Cessation

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Bupropion SRDrug

    Also called Wellbutrin SR, Zyban SR

    Comparison of bupropion SR or placebo + smoking cessation counseling

  • placeboDrug

  • smoking cessation counselingBehavioural

Study groups in NCT01875172
Study groupRoleWhat they receive
Bupropion SRExperimentalStudy 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.
Receives: Drug: Bupropion SR; Behavioral: smoking cessation counseling
PlaceboPlacebo comparatorStudy 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.
Receives: Drug: placebo; Behavioral: smoking cessation counseling

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. biologically verified smoking cessation or reduction

    change in smoking from study enrollment to end of treatment (8 weeks) and at delivery

    Measured: 8 weeks and delivery

Secondary outcomes (2)
  1. adverse events reported during pregnancy

    Measured: 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

    Measured: 8 weeks and delivery

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Jun 2013 (estimated)
  2. Study startOct 2001
  3. Primary completionJan 2004
  4. Study completionJan 2004

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
135 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01875172
Sponsor's protocol ID
1R21CA089510-01A2
Status last verified
Jun 2013
First submitted
14 Apr 2013
Last updated
11 Jun 2013
Results posted
No
Data monitoring committee
Yes

Publications

  • Hajizadeh A, Howes S, Theodoulou A, Klemperer E, Hartmann-Boyce J, Livingstone-Banks J, Lindson N. Antidepressants for smoking cessation. Cochrane Database Syst Rev. 2023 May 24;5(5):CD000031. doi: 10.1002/14651858.CD000031.pub6.

    PubMed 37230961

Questions about this trial

What is this clinical trial studying?

A Phase 2 study testing Bupropion SR and smoking cessation counseling in people with Smoking Cessation and Pregnancy, run by Watching Over Mothers & Babies Foundation at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 8 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Jun 2013. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 2 studies give the treatment to a larger group to see whether it has the intended effect and to keep checking safety.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

biologically verified smoking cessation or reduction (time frame: 8 weeks and delivery). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT01875172, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Jun 2013.

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