Safety and efficacy in parous women of a 52-mg levonorgestrel-medicated intrauterine device: a 7-year randomized comparative study with the TCu380A()()

OBJECTIVES: To compare rates of unintended pregnancy, method continuation and reasons for removal among women using the 52-mg levonorgestrel (daily release 20 microg) levonorgestrel IUD (LNG-IUD) or the copper T 380 A (TCu380A) intrauterine device. STUDY DESIGN: This was an open-label 7-year randomi...

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Detalles Bibliográficos
Autores principales: Rowe, Patrick, Farley, Tim, Peregoudov, Alexandre, Piaggio, Gilda, Boccard, Simone, Landoulsi, Sihem, Meirik, Olav
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Original Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357727/
https://www.ncbi.nlm.nih.gov/pubmed/26916172
http://dx.doi.org/10.1016/j.contraception.2016.02.024

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5357727/
https://www.ncbi.nlm.nih.gov/pubmed/26916172
http://dx.doi.org/10.1016/j.contraception.2016.02.024

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