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Completed No phase listed Observational Accepts healthy volunteers

KYleena Satisfaction Study / Observational Study on User Satisfaction With the Levonorgestrel Intrauterine Delivery System Kyleena (LNG-IUS 12) in New Contraceptive Users and After Switching From Another Contraceptive Method

ClinicalTrials.gov ID: NCT03182140

Public ClinicalTrials.gov record NCT03182140. 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 21, 2026, 8:31 PM EDT

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

Brief summary

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

The main goal of this non-interventional study (NIS) is to evaluate user satisfaction with Kyleena in a real-life setting and to identify factors which influence user satisfaction, taking into account previously used contraceptive methods and reasons for use of Kyleena.

Study identification

NCT ID
NCT03182140
Recruitment status
Completed
Study type
Observational
Phase
Not listed
Lead sponsor
Bayer
Industry
Enrollment
1,134 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
Not listed
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
Jul 6, 2017 (Actual)
Primary completion
Dec 19, 2019 (Actual)
Completion
Mar 31, 2020 (Actual)
Last update posted
Mar 29, 2021

2017 – 2020

United States locations

U.S. sites
12
U.S. states
10
U.S. cities
12
Facility City State ZIP Site status
Jennifer Grube, MD, FACOG Lakewood Colorado 80228 —
Physician Care Clinical Research LLC Sarasota Florida 34239 —
Visions Clinical Research Wellington Florida 33414 —
New England Center for Clinical Research Primacare Research, LLC Fall River Massachusetts 02721 —
Saginaw Valley Medical Research Group, LLC Saginaw Michigan 48604 —
Lawrence OB/GYN Clinical Research, LLC Lawrenceville New Jersey 08648 —
ProHEALTH Care Associates Port Jefferson New York 11777 —
Eastern Carolina Women's Center New Bern North Carolina 28562 —
Radiant Research Akron Ohio 44311 —
TMC Life Research Houston Texas 77054 —
Physician's Research Draper Utah 84020 —
Physician's Research Options LLC - Revere Women's Health OB/GYN Clinic Pleasant Grove Utah 84062 —

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03182140, 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 Mar 29, 2021 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03182140 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →