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COMPLETED NA

Smoking Cessation in Women With Gynecological Conditions

NCT01989923 · View on ClinicalTrials.gov ↗

Study Summary

This feasibility study will compare two smoking cessation methods, traditional nicotine replacement therapy and Electronic Nicotine Delivery Systems (electronic cigarettes) in patients with gynecological conditions.

Conditions Studied

Interventions

  • OTHER Nicotine Replacement Therapy
  • DEVICE Electronic Cigarettes

Study Locations (1)

Oklahoma

  • Stephenson Cancer Center — Oklahoma City

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2013-06
Est. Completion 2017-04-13
Phase NA

Sponsor

University of Oklahoma

306 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01989923

The ClinicalTrials.gov registry entry for NCT01989923 describes a study currently listed as completed. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Oklahoma, which has 306 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Cervical Dysplasia appearing as the primary indexed condition, and to 2 interventions — of which Nicotine Replacement Therapy is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01989923 reports 1 study location spanning 1 distinct geographic area — top geographies include Oklahoma. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01989923 about?

NCT01989923 is a clinical study titled "Smoking Cessation in Women With Gynecological Conditions". This feasibility study will compare two smoking cessation methods, traditional nicotine replacement therapy and Electronic Nicotine Delivery Systems (electronic cigarettes) in patients with gynecological conditions.

What is the current status of trial NCT01989923?

This trial is currently completed. It is a NA study. The enrollment target is 31 participants. The study started on 2013-06. Estimated completion is 2017-04-13.

What conditions does trial NCT01989923 study?

This clinical trial studies the following conditions: Cervical Dysplasia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01989923?

The interventions under investigation include: Nicotine Replacement Therapy (OTHER), Electronic Cigarettes (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01989923?

This trial is sponsored by University of Oklahoma, which has 306 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01989923 being conducted?

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

Related

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