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

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

sites

Many locations

Multiple Locations,

from

Multiple Locations,