Last updated on May 2018

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


Brief description of study

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.

Clinical Study Identifier: NCT03182140

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Bayer Clinical Trials Contact

Many locations
Multiple Locations, Belgium
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Jennifer Grube, MD, FACOG
Lakewood, CO United States
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Physician Care Clinical Research LLC
Sarasota, FL United States
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Visions Clinical Research
Wellington, FL United States
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New England Center for Clinical Research Primacare Research, LLC
Fall River, MA United States
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Saginaw Valley Medical Research Group, LLC
Saginaw, MI United States
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Lawrence OB/GYN Clinical Research, LLC
Lawrenceville, NJ United States
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ProHEALTH Care Associates
Port Jefferson, NY United States
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Eastern Carolina Women's Center
New Bern, NC United States
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Radiant Research
Akron, OH United States
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TMC Life Research
Houston, TX United States
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Physician's Research
Draper, UT United States
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Physician's Research Options LLC - Revere Women's Health OB/GYN Clinic
Pleasant Grove, UT United States
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