An Observational Study to Assess Quality of Life and Satisfaction of Young Women (Aged 18-29) Following 6 (±1) Months Using Jaydess as Their Contraceptive Method

CompletedOBSERVATIONAL

Enrollment

1,039

Participants

Timeline

Start Date

September 18, 2015

Primary Completion Date

July 1, 2016

Study Completion Date

September 28, 2016

Conditions

Quality of Life

Interventions

DRUG

Levonorgestrel (Jaydess, BAY86-5028)

Intrauterine delivery system Jaydess (13.5 mg levonorgestrel)

Trial Locations (1)

Many Locations