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Terminated Phase 3 Interventional Accepts healthy volunteers Results available

A Study of a Levonorgestrel-Releasing Intrauterine System for Long-Term, Reversible Contraception

ClinicalTrials.gov ID: NCT00995150

Public ClinicalTrials.gov record NCT00995150. 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 22, 2026, 1:51 AM 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 Phase 3, Multi-Center, Open-Label Study of a Levonorgestrel-Releasing Intrauterine System for Long-Term, Reversible Contraception

Brief summary

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

The primary objective of this study is to assess the efficacy of a levonorgestrel-releasing intrauterine system (LNG20) in nulliparous and parous females of child-bearing potential who request long-term, reversible contraception for up to 10 years.

Study identification

NCT ID
NCT00995150
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Medicines360
Other
Enrollment
1,910 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
16 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 2009 (Actual)
Primary completion
Oct 12, 2021 (Actual)
Completion
Oct 12, 2021 (Actual)
Last update posted
Aug 14, 2024

2009 – 2021

United States locations

U.S. sites
25
U.S. states
19
U.S. cities
25
Facility City State ZIP Site status
Not listed Phoenix Arizona — —
Not listed Palo Alto California — —
Not listed San Francisco California — —
Not listed Vista California — —
Not listed Denver Colorado — —
Not listed Atlanta Georgia — —
Not listed Idaho Falls Idaho — —
Not listed Chicago Illinois — —
Not listed Des Moines Iowa — —
Not listed Ann Arbor Michigan — —
Not listed St Louis Missouri — —
Not listed New York New York — —
Not listed Chapel Hill North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Cleveland Ohio — —
Not listed Columbus Ohio — —
Not listed Tulsa Oklahoma — —
Not listed Portland Oregon — —
Not listed Philadelphia Pennsylvania — —
Magee Women's Hospital, University of Pittsburgh Pittsburgh Pennsylvania 15213 —
Not listed Dallas Texas — —
Not listed Houston Texas — —
Not listed Salt Lake City Utah — —
Not listed Norfolk Virginia — —
Not listed Seattle Washington — —

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 NCT00995150, 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 Aug 14, 2024 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00995150 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →