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Completed Not applicable Interventional Accepts healthy volunteers

Evaluation of Safety and Effectiveness of the Essure (Model ESS505) Device to Prevent Pregnancy in Women

ClinicalTrials.gov ID: NCT01948882

Public ClinicalTrials.gov record NCT01948882. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 9:39 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Multi-National Clinical Study to Evaluate the Safety and Effectiveness of the Essure® (Model ESS505) Device to Prevent Pregnancy in Women Who Are Seeking Permanent Contraception

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The Essure System is indicated for women who desire non-incisional permanent birth control (female sterilization) by occlusion of the fallopian tubes. The objective of the study is to evaluate the safety and effectiveness of the Essure System (Model ESS505) for permanent birth control in preventing pregnancy. The Essure ESS505 System includes a design modification that will be studied to determine if it provides immediate birth control, thereby removing the three months waiting period required for the commercially available Essure System Model 305 to be effective.

Study identification

NCT ID
NCT01948882
Recruitment status
Completed
Study type
Interventional
Phase
Not applicable
Lead sponsor
Bayer
Industry
Enrollment
660 participants

Conditions and interventions

Conditions

Interventions

Device

Eligibility (public fields only)

Age range
21 Years to 44 Years
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 30, 2013 (Actual)
Primary completion
Sep 16, 2015 (Actual)
Completion
Sep 12, 2024 (Actual)
Last update posted
Oct 17, 2024

2013 – 2024

United States locations

U.S. sites
17
U.S. states
11
U.S. cities
17
Facility City State ZIP Site status
Not listed Aurora Colorado 80045 —
Not listed Denver Colorado 80231 —
Not listed Wellington Florida 33414 —
Not listed Fort Wayne Indiana 46825 —
Not listed Newburgh Indiana 47630 —
Not listed Saginaw Michigan 48604 —
Not listed Rochester Minnesota 55905 —
Not listed New York New York 10032 —
Not listed The Bronx New York 10467 —
Not listed Asheville North Carolina 28801 —
Not listed Cincinnati Ohio 45242 —
Not listed Columbia Ohio 60004 —
Not listed Dallas Texas 75208 —
Not listed Houston Texas 77074 —
Not listed Irving Texas 75062 —
Not listed Norfolk Virginia 23507 —
Not listed Spokane Washington 99204 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01948882, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 17, 2024 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01948882 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →