Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT04670822 · ClinicalTrials.gov registry record · NA

Postpartum Smoking Relapse Prevention by Breastfeeding Promotion

A NA study, sponsored by State University of New York at Buffalo.

Completed
Registry status
NA
Development phase
60
Enrollment target

NCT04670822: Completed NA study, sponsored by State University of New York at Buffalo.

NCT04670822 is a NA study that has completed, run by State University of New York at Buffalo. The registered enrollment target is 60 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04670822, a NA study, has completed, sponsored by State University of New York at Buffalo.

COMPLETED
Registry status
NA
Development phase
60 participants
Enrollment target

Study Summary

This is a randomized controlled trial to prevent postpartum smoking relapse by breastfeeding promotion. The intervention group (N=30) will receive multicomponent breastfeeding intervention from late pregnancy to 6 months postpartum, while the attention placebo control group (N=30) will receive general infant care counseling and support. The key outcome is the rate of postpartum smoking relapse.

Primary Outcome

During postpartum, mothers report their breastfeeding status (exclusive, mixed with formula, non-breastfeeding) every month until 9 months postpartum. Any breastfeeding is defined as exclusive breastfeeding or mixed-feeding breast milk and formula.

Interventions

  • BEHAVIORAL Breastfeeding promotion
  • BEHAVIORAL Attention placebo control

Trial Details

FieldValue
Enrollment Target 60 participants
Start Date 2018-07-31
Est. Completion 2023-12-31
Phase NA

What the finished NCT04670822 record still lists

NCT04670822 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 60 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (96% lower).

The record links to 0 conditions, and to 2 interventions - of which Breastfeeding promotion is the first listed.

NCT04670822 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT04670822 about?

NCT04670822 is a clinical study titled "Postpartum Smoking Relapse Prevention by Breastfeeding Promotion". This is a randomized controlled trial to prevent postpartum smoking relapse by breastfeeding promotion. The intervention group (N=30) will receive multicomponent breastfeeding intervention from late pregnancy to 6 months postpartum, while the attention placebo control group (N=30) will receive gener...

What is the current status of trial NCT04670822?

This trial is currently completed. It is a NA study. The enrollment target is 60 participants. The study started on 2018-07-31. Estimated completion is 2023-12-31.

What interventions are being tested in trial NCT04670822?

The interventions under investigation include: Breastfeeding promotion (BEHAVIORAL), Attention placebo control (BEHAVIORAL).

Who is sponsoring clinical trial NCT04670822?

This trial is sponsored by State University of New York at Buffalo, which has 243 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT04670822's enrollment target sits among peer trials

60 1164th of 2000 higher than 745 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00576069 · 60 participants

    Mechanism(s)of Airflow Limitation in Moderate-severe Persistent Asthma

  • NCT01297400 · 60 participants · Phase 2

    Phase 2 Pilot Study of the Safety and Efficacy of Topical MW-III in Thermal Burns

  • NCT01734122 · 60 participants

    Stereotactic Radiosurgery for Essential Tremor and Parkinsonian Tremor

  • NCT01804634 · 60 participants · Phase 2

    Reduced Intensity Haploidentical BMT for High Risk Solid Tumors

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT04670822, the US trial registry maintained by the National Library of Medicine. NCT04670822 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.