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

NCT04783857 · ClinicalTrials.gov registry record · Phase 4

Modifying Progesterone and Estradiol Levels to Prevent Postpartum Cigarette Smoking Relapse and Reduce Secondhand Smoke Exposure in Infants and Children

A Phase 4 study of Smoking Cessation and Smoking, sponsored by University of Minnesota.

Recruiting
Registry status
Phase 4
Development phase
279
Enrollment target
1
Study location

NCT04783857 is a Phase 4 study of Smoking Cessation and Smoking that is actively recruiting participants, run by University of Minnesota. The registered enrollment target is 279 participants, below the 473-participant average among 188 other Smoking Cessation trials with a reported enrollment target (41% lower). The trial reports 1 study location across 1 state.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT04783857, a Phase 4 study of Smoking Cessation and Smoking, is actively recruiting participants, sponsored by University of Minnesota.

RECRUITING
Registry status
Phase 4
Development phase
279 participants
Enrollment target
1
Study location

Study Summary

The investigators aim to address the following specific aims: * Determine the efficacy of Prog in preventing postpartum smoking relapse and reducing smoking relapse risk factors. * Examine the effects of this maternal smoking intervention on infant health. * Examine racial and ethnic differences in intervention outcomes.

Interventions

  • DRUG Progesterone 200 MG Oral Capsule

Study Locations (1)

Minnesota

  • University of Minnesota - Minneapolis

Trial Details

FieldValue
Enrollment Target 279 participants
Start Date 2022-04-14
Est. Completion 2026-06-02
Phase Phase 4

Sponsor

University of Minnesota

966 total trials

What the Registry Record Tells You About NCT04783857

The ClinicalTrials.gov registry entry for NCT04783857 describes a study currently listed as recruiting, categorized as Phase 4. The registered enrollment target is 279 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 473-participant average among 188 other Smoking Cessation trials with a reported enrollment target (41% lower). The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Smoking Cessation appearing as the primary indexed condition, and to 1 intervention - of which Progesterone 200 MG Oral Capsule is the first listed.

NCT04783857 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT04783857 about?

NCT04783857 is a clinical study titled "Modifying Progesterone and Estradiol Levels to Prevent Postpartum Cigarette Smoking Relapse and Reduce Secondhand Smoke Exposure in Infants and Children". The investigators aim to address the following specific aims: * Determine the efficacy of Prog in preventing postpartum smoking relapse and reducing smoking relapse risk factors. * Examine the effects of this maternal smoking intervention on infant health. * Examine racial and ethnic differences in...

What is the current status of trial NCT04783857?

This trial is currently recruiting. It is a Phase 4 study. The enrollment target is 279 participants. The study started on 2022-04-14. Estimated completion is 2026-06-02.

What conditions does trial NCT04783857 study?

This clinical trial studies the following conditions: Smoking Cessation, Smoking, Smoking Reduction.

What interventions are being tested in trial NCT04783857?

The interventions under investigation include: Progesterone 200 MG Oral Capsule (DRUG).

Who is sponsoring clinical trial NCT04783857?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT04783857 being conducted?

This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Smoking Cessation

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.