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NCT01989923 · ClinicalTrials.gov registry record · NA

Smoking Cessation in Women With Gynecological Conditions

A NA study of Cervical Dysplasia, sponsored by University of Oklahoma.

Completed
Registry status
NA
Development phase
31
Enrollment target
1
Study location

NCT01989923 is a NA study of Cervical Dysplasia that has completed, run by University of Oklahoma. The registered enrollment target is 31 participants, below the 545-participant average among 7 other Cervical Dysplasia trials with a reported enrollment target (94% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT01989923, a NA study of Cervical Dysplasia, has completed, sponsored by University of Oklahoma.

COMPLETED
Registry status
NA
Development phase
31 participants
Enrollment target
1
Study location

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

358 total trials

What the Registry Record Tells You About NCT01989923

The ClinicalTrials.gov registry entry for NCT01989923 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 545-participant average among 7 other Cervical Dysplasia trials with a reported enrollment target (94% lower). The listed sponsor is University of Oklahoma, which has 358 total studies on file at ClinicalTrials.gov.

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.

NCT01989923 reports 1 study location spanning 1 distinct geographic area - top geographies include Oklahoma.

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.

What interventions are being tested in trial NCT01989923?

The interventions under investigation include: Nicotine Replacement Therapy (OTHER), Electronic Cigarettes (DEVICE).

Who is sponsoring clinical trial NCT01989923?

This trial is sponsored by University of Oklahoma, which has 358 total clinical trials registered on ClinicalTrials.gov.

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.

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