findmyKOL
Clinical trialNCT01177670TerminatedObservational

Adiana Post-Approval Clinical Study (APACS)

SponsorHologic, Inc.Enrollment169Women Contraception
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

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.
clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

9 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • Sutter Medical Group

    Elk Grove, California, United States

  • Womencare, P.C.

    Arlington Heights, Illinois, United States

  • University of Missouri Health Care

    Columbia, Missouri, United States

  • Valaoras & Lewis Obstetrics and Gynecology

    Winston-Salem, North Carolina, United States

  • Complete Healthcare for Women

    Columbus, Ohio, United States

  • the Women'S Center of Central Oregon

    Redmond, Oregon, United States

  • Salem Women'S Clinic

    Salem, Oregon, United States

  • Western Pennsylvania Hospital

    Pittsburgh, Pennsylvania, United States

  • Ob/gyn Associates of Danville

    Danville, Virginia, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

No drug or biological interventions are in our data for this study — it may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Aug 2010
Primary completion
—
Completion
30 Apr 2012
Last update posted
20 Nov 2012
Registered enrollment
169
Registry id
NCT01177670
clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.