Efficacy and Safety Study of Norethindrone Acetate Transdermal Delivery System in Contraception (Simplify)

September 13, 2013 updated by: Watson Pharmaceuticals

An Open Label Study to Evaluate the Contraceptive Efficacy and Safety of Norethindrone Acetate Transdermal Delivery System

The purpose of this study is to determine whether NEA TDS is effective in the prevention of pregnancy. The safety of this product will also be evaluated.

Study Overview

Status

Status

Indicates the current recruitment status or the expanded access status.
Completed

Conditions

Conditions

The disease, disorder, syndrome, illness, or injury that is being studied. On ClinicalTrials.gov, conditions may also include other health-related issues, such as lifespan, quality of life, and health risks.

Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.

Detailed Description

An Open Label Study to Evaluate the Contraceptive Efficacy and Safety of Norethindrone Acetate Transdermal Delivery System.

Study Type

Study Type

Describes the nature of a clinical study. Study types include interventional studies (also called clinical trials), observational studies (including patient registries), and expanded access.
Interventional

Enrollment (Actual)

Enrollment

The number of participants in a clinical study. The "anticipated" enrollment is the target number of participants that the researchers need for the study.
1659

Phase

Phase

The stage of a clinical trial studying a drug or biological product, based on definitions developed by the U.S. Food and Drug Administration (FDA). The phase is based on the study's objective, the number of participants, and other characteristics. There are five phases: Early Phase 1 (formerly listed as Phase 0), Phase 1, Phase 2, Phase 3, and Phase 4. Not Applicable is used to describe trials without FDA-defined phases, including trials of devices or behavioral interventions.
  • Phase 3

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

  • United States
    • Alabama
      • Birmingham, Alabama, United States
        • Watson Investigational Site
      • Mobile, Alabama, United States
        • Watson Investigational Site
      • Montgomery, Alabama, United States
        • Watson Investigational Site
    • Arizona
      • Chandler, Arizona, United States
        • Watson Investigational Site
    • Arkansas
      • Little Rock, Arkansas, United States
        • Watson Investigational Site
    • California
      • Garden Grove, California, United States
        • Watson Investigational Site
      • La Mesa, California, United States
        • Watson Investigational Site
      • San Diego, California, United States
        • Watson Investigational Site
    • Colorado
      • Denver, Colorado, United States
        • Watson Investigational Site
    • Delaware
      • Newark, Delaware, United States
        • Watson Investigational Site
    • District of Columbia
      • Washington, District of Columbia, United States
        • Watson Investigational Site
    • Florida
      • Aventura, Florida, United States
        • Watson Investigational Site
      • Daytona Beach, Florida, United States
        • Watson Investigational Site
      • Jacksonville, Florida, United States
        • Watson Investigational Site
      • Lake Worth, Florida, United States
        • Watson Investigational Site
      • Miami, Florida, United States
        • Watson Investigational Site
      • North Miami, Florida, United States
        • Watson Investigational Site
      • Pinellas Park, Florida, United States
        • Watson Investigational Site
      • Sarasota, Florida, United States
        • Watson Investigational Site
    • Georgia
      • Atlanta, Georgia, United States
        • Watson Investigational Site
      • Decatur, Georgia, United States
        • Watson Investigational Site
      • Sandy Springs, Georgia, United States
        • Watson Investigational Site
      • Savannah, Georgia, United States
        • Watson Investigational Site
    • Illinois
      • Chicago, Illinois, United States
        • Watson Investigational Site
    • Kansas
      • Overland Park, Kansas, United States
        • Watson Investigational Site
    • Louisiana
      • Marrero, Louisiana, United States
        • Watson Investigational Site
      • New Orleans, Louisiana, United States
        • Watson Investigational Site
    • Massachusetts
      • Haverhill, Massachusetts, United States
        • Watson Investigational Site
    • Michigan
      • Ann Arbor, Michigan, United States
        • Watson Investigational Site
      • Kalamazoo, Michigan, United States
        • Watson Investigational Site
    • Minnesota
      • Edina, Minnesota, United States
        • Watson Investigational Site
    • Nevada
      • Las Vegas, Nevada, United States
        • Watson Investigational Site
    • New Jersey
      • Lawrenceville, New Jersey, United States
        • Watson Investigational Site
    • New Mexico
      • Albuquerque, New Mexico, United States
        • Watson Investigational Site
    • New York
      • New York, New York, United States
        • Watson Investigational Site
    • North Carolina
      • Chapel Hill, North Carolina, United States
        • Watson Investigational Site
      • New Bern, North Carolina, United States
        • Watson Investigational Site
      • Raleigh, North Carolina, United States
        • Watson Investigational Site
    • Ohio
      • Cleveland, Ohio, United States
        • Watson Investigational Site
      • Columbus, Ohio, United States
        • Watson Investigational Site
    • Oregon
      • Medford, Oregon, United States
        • Watson Investigational Site
    • Pennsylvania
      • Philadelphia, Pennsylvania, United States
        • Watson Investigational Site
    • South Carolina
      • Columbia, South Carolina, United States
        • Watson Investigational Site
      • Greer, South Carolina, United States
        • Watson Investigational Site
      • Hilton Head Island, South Carolina, United States
        • Watson Investigational Site
    • Tennessee
      • Nashville, Tennessee, United States
        • Watson Investigational Site
    • Texas
      • Austin, Texas, United States
        • Watson Investigational Site
      • Dallas, Texas, United States
        • Watson Investigational Site
      • Houston, Texas, United States
        • Watson Investigational Site
      • San Antonio, Texas, United States
        • Watson Investigational Site
    • Utah
      • Salt Lake City, Utah, United States
        • Watson Investigational Site
    • Virginia
      • Norfolk, Virginia, United States
        • Watson Investigational Site
    • Washington
      • Seattle, Washington, United States
        • Watson Investigational Site

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Eligibility Criteria

The key requirements that people who want to participate in a clinical study must meet or the characteristics they must have. Eligibility criteria consist of both inclusion criteria (which are required for a person to participate in the study) and exclusion criteria (which prevent a person from participating). Types of eligibility criteria include whether a study accepts healthy volunteers, has age or age group requirements, or is limited by sex.

Ages Eligible for Study

18 years to 45 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Healthy females
  • 18-45 years
  • Regular, consistent menstrual cycles between 25 and 35 days
  • Sexually active and at risk of becoming pregnant

Exclusion Criteria:

  • History of infertility
  • Known contraindications to progestogen administration
  • Pap smear suggestive of a high-grade precancerous lesion(s)
  • Clinically significant deviation from normal in any of the screening tests or exams

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm

Participant Group / Arm

A group or subgroup of participants in a clinical trial that receives a specific intervention/treatment, or no intervention, according to the trial's protocol.
Intervention / Treatment

Intervention / Treatment

A process or action that is the focus of a clinical study. Interventions include drugs, medical devices, procedures, vaccines, and other products that are either investigational or already available. Interventions can also include noninvasive approaches, such as education or modifying diet and exercise.
Experimental: Active treatment
Norethindrone Acetate Transdermal Delivery System
Drug: Norethindrone Acetate
Norethindrone Acetate Transdermal Delivery System
Other Names:
  • NEA TDS

What is the study measuring?

Primary Outcome Measures

Primary Outcome Measures

In a clinical study's protocol, the planned outcome measure that is the most important for evaluating the effect of an intervention/treatment. Most clinical studies have one primary outcome measure, but some have more than one.
Outcome Measure
Measure Description
Time Frame
Pregnancy Rate
Time Frame: 1 year
The pregnancy rate will be calculated using the Pearl Index that defined as 1300*Number of pregnancies/Number of cycles of treatment.
1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Sponsor

The organization or person who initiates the study and who has authority and control over the study.
Watson Pharmaceuticals

Investigators

Investigators

A researcher involved in a clinical study. Related terms include site principal investigator, site sub-investigator, study chair, study director, and study principal investigator.
  • Study Director: Kim E Caramelli, MS, Watson Pharmaceuticals, Inc.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

Study Start

The actual date on which the first participant was enrolled in a clinical study. The "anticipated" study start date is the date that the researchers think will be the study start date.
May 1, 2010

Primary Completion (Actual)

Primary Completion

The date on which the last participant in a clinical study was examined or received an intervention to collect final data for the primary outcome measure. Whether the clinical study ended according to the protocol or was terminated does not affect this date. For clinical studies with more than one primary outcome measure with different completion dates, this term refers to the date on which data collection is completed for all the primary outcome measures. The "anticipated" primary completion date is the date that the researchers think will be the primary completion date for the study.
March 1, 2012

Study Completion (Actual)

Study Completion

The date on which the last participant in a clinical study was examined or received an intervention/treatment to collect final data for the primary outcome measures, secondary outcome measures, and adverse events (that is, the last participant's last visit). The "anticipated" study completion date is the date that the researchers think will be the study completion date.
March 1, 2012

Study Registration Dates

First Submitted

First Submitted

The date on which the study sponsor or investigator first submitted a study record to ClinicalTrials.gov. There is typically a delay of a few days between the first submitted date and the record's availability on ClinicalTrials.gov (the first posted date).
May 18, 2010

First Submitted That Met QC Criteria

First Submitted That Met QC Criteria

The date on which the study sponsor or investigator first submits a study record that is consistent with National Library of Medicine (NLM) quality control (QC) review criteria. The sponsor or investigator may need to revise and submit a study record one or more times before NLM's QC review criteria are met. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
June 7, 2010

First Posted (Estimate)

First Posted

The date on which the study record was first available on ClinicalTrials.gov after National Library of Medicine (NLM) quality control (QC) review has concluded. There is typically a delay of a few days between the date the study sponsor or investigator submitted the study record and the first posted date.
June 9, 2010

Study Record Updates

Last Update Posted (Estimate)

Last Update Posted

The most recent date on which changes to a study record were made available on ClinicalTrials.gov. There may be a delay between when the changes were submitted to ClinicalTrials.gov by the study's sponsor or investigator (the last update submitted date) and the last update posted date.
September 19, 2013

Last Update Submitted That Met QC Criteria

Last Update Submitted That Met QC Criteria

The most recent date on which the study sponsor or investigator submitted changes to a study record that are consistent with National Library of Medicine (NLM) quality control (QC) review criteria. It is the responsibility of the sponsor or investigator to ensure that the study record is consistent with the NLM QC review criteria.
September 13, 2013

Last Verified

Last Verified

The most recent date on which the study sponsor or investigator confirmed the information about a clinical study on ClinicalTrials.gov as accurate and current. If a study with a recruitment status of recruiting; not yet recruiting; or active, not recruiting has not been confirmed within the past 2 years, the study's recruitment status is shown as unknown.
September 1, 2013

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

Other Study ID Numbers

Identifiers or ID numbers other than the NCT number that are assigned to a clinical study by the study's sponsor, funders, or others. These numbers may include unique identifiers from other trial registries and National Institutes of Health grant numbers.
  • NE0906

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Cookie Settings

We use cookies to ensure that we give you the best experience on our website. For more details carefully read our Privacy and Cookies Policy. ...>>>You can change your preferences or withdraw your consent at any time by deleting the cookies from your website or computer as described in the policy. Please accept it and choose your preferences by ticking the corresponding boxes in the "Manage Settings" section below. Please carefully read our Terms of Service before you proceed with using any part of this website.
«Manage Settings