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



Status:Active, not recruiting
Conditions:Contraception, Contraception
Therapuetic Areas:Reproductive
Healthy:No
Age Range:Any
Updated:3/27/2019
Start Date:July 7, 2017
End Date:March 30, 2020

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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.


Inclusion Criteria:

- Women requesting contraception with Kyleena. The woman's informed decision for
contraception with Kyleena was made before and independently from the study as per
investigator's routine practice

- Written informed consent.

Exclusion Criteria:

- Contraindications for Kyleena according to the local market authorization/SmPC

- Mental incapacity to consent and provide data during the observational study

- Women participating in an investigational program with interventions outside of
routine clinical practice.
We found this trial at
13
sites
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Pleasant Grove, UT
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Akron, Ohio 44311
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Akron, OH
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Draper, Utah 84020
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from
Draper, UT
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from
Fall River, MA
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Houston, Texas 77054
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from
Houston, TX
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Lakewood, Colorado 80228
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from
Lakewood, CO
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Lawrenceville, New Jersey 08648
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from
Lawrenceville, NJ
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Multiple Locations,
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from
Multiple Locations,
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New Bern, North Carolina 28562
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from
New Bern, NC
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Port Jefferson, New York 11777
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from
Port Jefferson, NY
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from
Saginaw, MI
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Sarasota, Florida 34321
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from
Sarasota, FL
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Wellington, Florida 33414
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from
Wellington, FL
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