Safety and Contraceptive Efficacy of an Intravaginal Ring With LNG (Levonorgestrel) Over One Year in Healthy Women

April 6, 2021 updated by: Bayer

Multi-center, Open-label, Single-arm Study to Assess the Safety and Contraceptive Efficacy of a Levonorgestrel-containing Intravaginal Ring During a Treatment Period of One Year in Healthy Women 18 to 35 Years of Age

Purpose of the study is to investigate safety and contraceptive efficacy of an LNG-containing intravaginal ring.

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.

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.
1471

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

  • Japan
      • Fukui, Japan, 910-8561
      • Fukui, Japan, 910-0845
      • Fukui, Japan, 910-0858
      • Fukuoka, Japan, 813-0017
      • Osaka, Japan, 530-0013
      • Osaka, Japan, 542-0086
      • Osaka, Japan, 542-0081
    • Chiba
      • Funabashi, Chiba, Japan, 274-0071
      • Yotsukaido, Chiba, Japan, 284-0001
    • Hiroshima
      • Aki-gun, Hiroshima, Japan, 735-0029
    • Hokkaido
      • Sapporo, Hokkaido, Japan, 060-0807
      • Sapporo, Hokkaido, Japan, 004-0004
    • Okayama
      • Kurashiki, Okayama, Japan, 710-0824
    • Tokyo
      • Chuo-ku, Tokyo, Japan, 104-0061
      • Hachioji, Tokyo, Japan, 192-0046
      • Nakano-ku, Tokyo, Japan, 165-0032
      • Nishitokyo, Tokyo, Japan, 188-0011
      • Ota-ku, Tokyo, Japan, 144-0052
      • Setagaya-ku, Tokyo, Japan, 156-0042
      • Shinjuku, Tokyo, Japan, 162-0053
      • Toshima-ku, Tokyo, Japan, 171-0021
  • United States
    • Alabama
      • Mobile, Alabama, United States, 36608
    • Arizona
      • Chandler, Arizona, United States, 85224
      • Mesa, Arizona, United States, 85209
      • Phoenix, Arizona, United States, 85032
      • Tucson, Arizona, United States, 85710
    • Arkansas
      • Little Rock, Arkansas, United States, 72205
    • California
      • La Mesa, California, United States, 91942
      • Sacramento, California, United States, 95821
      • Sacramento, California, United States, 95822
      • San Diego, California, United States, 92103
      • San Diego, California, United States, 92108
      • San Diego, California, United States, 92123
    • Colorado
      • Denver, Colorado, United States, 80218
      • Denver, Colorado, United States, 80220
    • Connecticut
      • New London, Connecticut, United States, 06320
    • Florida
      • Clearwater, Florida, United States, 33759
      • Jacksonville, Florida, United States, 32216
      • Jupiter, Florida, United States, 33458
      • Lake Worth, Florida, United States, 33461
      • Leesburg, Florida, United States, 34748
      • Miami, Florida, United States, 33186
      • Miami Beach, Florida, United States, 33141
      • North Miami, Florida, United States, 33161
      • Oviedo, Florida, United States, 32765
      • Saint Petersburg, Florida, United States, 33709
      • Wellington, Florida, United States, 33414
    • Georgia
      • Atlanta, Georgia, United States, 30342
      • Roswell, Georgia, United States, 30075
    • Idaho
      • Idaho Falls, Idaho, United States, 83404
    • Illinois
      • Champaign, Illinois, United States, 61820
      • Chicago, Illinois, United States, 60610
    • Kansas
      • Shawnee Mission, Kansas, United States, 66218
      • Wichita, Kansas, United States, 67207
    • Maryland
      • Baltimore, Maryland, United States
      • Lutherville, Maryland, United States, 21093
    • Missouri
      • Kansas City, Missouri, United States, 64114
    • Nebraska
      • Lincoln, Nebraska, United States, 68510
    • Nevada
      • Las Vegas, Nevada, United States, 89109
      • Las Vegas, Nevada, United States, 89128
      • Las Vegas, Nevada, United States, 89104
    • New Jersey
      • Lawrenceville, New Jersey, United States, 08648
      • New Brunswick, New Jersey, United States, 08901
    • New Mexico
      • Albuquerque, New Mexico, United States, 87109
    • New York
      • Johnson City, New York, United States, 13790
      • Port Jefferson, New York, United States, 11777
      • Rochester, New York, United States, 14618
      • Williamsville, New York, United States, 14221
    • North Carolina
      • Cary, North Carolina, United States, 27518
      • Charlotte, North Carolina, United States, 28209
      • Durham, North Carolina, United States, 27713
      • Greensboro, North Carolina, United States, 27408
      • New Bern, North Carolina, United States, 28562
      • Raleigh, North Carolina, United States, 27607
      • Raleigh, North Carolina, United States, 27612
      • Salisbury, North Carolina, United States, 28144
      • Wilmington, North Carolina, United States, 28401
      • Winston-Salem, North Carolina, United States, 27103
    • Ohio
      • Cincinnati, Ohio, United States, 45267-0457
      • Cleveland, Ohio, United States, 44122
      • Columbus, Ohio, United States, 43213
    • Pennsylvania
      • Philadelphia, Pennsylvania, United States, 19114
      • Pittsburgh, Pennsylvania, United States, 15206
      • Pittsburgh, Pennsylvania, United States, 15213
    • South Carolina
      • Columbia, South Carolina, United States, 29201
      • Mount Pleasant, South Carolina, United States, 29464
      • Myrtle Beach, South Carolina, United States, 29572
      • Summerville, South Carolina, United States, 29485
    • Tennessee
      • Jackson, Tennessee, United States, 38305-3618
    • Texas
      • Corpus Christi, Texas, United States, 78414
      • Houston, Texas, United States, 77030
      • Houston, Texas, United States, 77074
      • San Antonio, Texas, United States, 78229
    • Utah
      • Draper, Utah, United States, 84020
      • Pleasant Grove, Utah, United States, 84107
      • Salt Lake City, Utah, United States, 84107
    • Virginia
      • Richmond, Virginia, United States, 23233
      • Virginia Beach, Virginia, United States, 23456
    • Washington
      • Seattle, Washington, United States, 98105
      • Spokane, Washington, United States, 99207

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 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  • Healthy female subject requesting contraception and willing to use the IVR
  • Normal or clinically insignificant cervical smear not requiring further follow up (a cervical smear has to be taken at screening visit or a normal result has to be documented within the previous 6 months)
  • History of regular cyclic menstrual periods
  • Subject is willing and able to attend the scheduled study visits and comply with study procedures

Exclusion Criteria:

  • Pregnancy or lactation (less than three months since delivery, abortion, or lactation before start of treatment)
  • Any diseases or conditions that can compromise the function of the body systems and could result in altered absorption, excessive accumulation, impaired metabolism, or altered excretion of the study drug
  • Any diseases or conditions that might interfere with the conduct of the study or the interpretation of the results
  • Any disease or condition that may worsen under hormonal treatment according to the assessment and opinion of the investigator
  • Undiagnosed abnormal genital bleeding
  • Wish for pregnancy during the study
  • Major surgery scheduled during the study period

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: Levonorgestrel (BAY98-7196)
Vaginal ring containing 170 mg levonorgestrel
Drug: Levonorgestrel (BAY98-7196)
Levonorgestrel 40 µg/d intravaginal ring (treatment for 365 days, 28 days wearing period for each ring)

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 (Pearl Index)
Time Frame: Up to 12 months
Pearl Index = Number of pregnancies per 100 woman-years of exposure
Up to 12 months

Secondary Outcome Measures

Secondary Outcome Measures

In a clinical study's protocol, a planned outcome measure that is not as important as the primary outcome measure for evaluating the effect of an intervention but is still of interest. Most clinical studies have more than one secondary outcome measure.
Outcome Measure
Measure Description
Time Frame
Cumulative failure rate
Time Frame: Up to 12 months
Probability of getting pregnant
Up to 12 months

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.
Bayer

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Helpful Links

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 (Actual)

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 15, 2015

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.
July 7, 2016

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.
July 7, 2016

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).
March 26, 2015

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.
March 26, 2015

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.
March 31, 2015

Study Record Updates

Last Update Posted (Actual)

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.
April 8, 2021

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.
April 6, 2021

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.
April 1, 2021

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.
  • 16803

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

Yes

Studies a U.S. FDA-regulated device product

No

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.

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