Regulatory Post Marketing Surveillance Study in Korea
Status:
Completed
Trial end date:
2017-08-11
Target enrollment:
Participant gender:
Summary
The objective of the study is to investigate and collect post marketing data on the safety
and efficacy of Visanne at follow-up visit after about 6 months of treatment and - for a
subset of patients - at optional long-term follow-up visit after about 1 year of treatment
under daily practice treatment conditions in Korean women and to obtain data on drug
utilization on treatment for endometriosis.