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Terminated No phase listed Observational Accepts healthy volunteers Results available

Adiana Post-Approval Clinical Study (APACS)

ClinicalTrials.gov ID: NCT01177670

Public ClinicalTrials.gov record NCT01177670. 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, 10:00 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Adiana Post-Approval Clinical Study

Brief summary

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

The Adiana Post-Approval Clinical Study (APACS) has been designed to compile information on the efficacy and safety of the Adiana Permanent Contraception System in the post market setting. Specifically, data will be collected that is relevant to the evaluation of the safety and efficacy of the Adiana System for women who desire permanent birth control by occlusion of the fallopian tubes. This study is an observational study that is not intended to test specific hypotheses.

Study identification

NCT ID
NCT01177670
Recruitment status
Terminated
Study type
Observational
Phase
Not listed
Lead sponsor
Hologic, Inc.
Industry
Enrollment
169 participants

Conditions and interventions

Interventions

Not listed

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
Aug 2010 (Type not available)
Primary completion
Not listed
Completion
Apr 2012 (Actual)
Last update posted
Nov 20, 2012

2010 – 2012

United States locations

U.S. sites
9
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Sutter Medical Group Elk Grove California 95758 —
WomenCare, P.C. Arlington Heights Illinois 60004 —
University of Missouri Health Care Columbia Missouri 65203 —
Valaoras & Lewis Obstetrics and Gynecology Winston-Salem North Carolina 27103 —
Complete Healthcare for Women Columbus Ohio 43231 —
The Women's Center of Central Oregon Redmond Oregon 97756 —
Salem Women's Clinic Salem Oregon 97302 —
Western Pennsylvania Hospital Pittsburgh Pennsylvania 15224 —
Ob/Gyn Associates of Danville Danville Virginia 24541 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01177670, 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 Nov 20, 2012 · 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 NCT01177670 live on ClinicalTrials.gov.

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