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Terminated Not applicable Interventional Accepts healthy volunteers Results available

Safety & Efficacy Study of the Adiana System for Women Who Desire Permanent Birth Control (Sterilization)

ClinicalTrials.gov ID: NCT00737061

Public ClinicalTrials.gov record NCT00737061. 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 Nov 7, 2026, 9:41 AM EST

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Official title

A Multi-Center, Prospective Evaluation of the Adiana System for Transcervical Sterilization Using Electrothermal Energy in Women Aged 18-45 - The EASE Trial

Brief summary

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

The purpose of this study is to demonstrate the safety \& efficacy of the Adiana Transcervical Sterilization System for women who desire permanent birth control (female sterilization) by occlusion of the fallopian tubes.

Study identification

NCT ID
NCT00737061
Recruitment status
Terminated
Study type
Interventional
Phase
Not applicable
Lead sponsor
Hologic, Inc.
Industry
Enrollment
770 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 45 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
Nov 2002 (Type not available)
Primary completion
Dec 2005 (Actual)
Completion
Feb 4, 2013 (Actual)
Last update posted
Sep 8, 2017

2002 – 2013

United States locations

U.S. sites
14
U.S. states
12
U.S. cities
14
Facility City State ZIP Site status
Women's Health Research Phoenix Arizona 85015 —
Kaiser Permanente Roseville California 95661 —
Kaiser Permanente San Rafael California 94903 —
Reproductive Science Center San Ramon California 94583 —
Center for Fertility and Women's Health New Britain Connecticut 06050 —
Institute for Women's Health and Body Wellington Florida 33414 —
Center for Reproductive Medicine Wichita Kansas 67226 —
Newton-Wellesley Hospital Newton Massachusetts 02462 —
Minnesota Gynecology and Surgery Edina Minnesota 55435 —
St. Luke's Hospital Chesterfield Missouri 63017 —
Duke Fertility Center Durham North Carolina 27713 —
Vanderbilt University Medical Center Nashville Tennessee 37232 —
Baylor Research Institute Fort Worth Texas 76104 —
Reproductive Specialty Center Milwaukee Wisconsin 53211 —

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 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00737061, 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 Sep 8, 2017 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00737061 live on ClinicalTrials.gov.

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