Acceptability of randomization to levonorgestrel versus copper intrauterine device among women requesting IUD insertion for contraception. Academic Article uri icon

Overview

abstract

  • OBJECTIVE: Assess feasibility of randomizing women to intrauterine device (IUD) type. STUDY DESIGN: Women enrolling in a 2-month study who desired an IUD for contraception were randomized 1:1 to receive a levonorgestrel-releasing 52-mg IUD (LNG-IUD) or copper T380A IUD (Cu-IUD), understanding they could switch IUD type at the end of the study. RESULTS: Randomization to IUD type was acceptable to 54/55 (98%) women who screened. All 32 enrolled participants completed follow-up. Two women exchanged their IUD (Cu-IUD to LNG-IUD), and two requested removal (one LNG-IUD, one Cu-IUD). Overall, 88% continued their assigned IUD. CONCLUSIONS: Randomization to IUD type is feasible, and few women change their IUD.

publication date

  • August 18, 2015

Research

keywords

  • Contraception
  • Contraceptive Agents, Female
  • Intrauterine Devices, Copper
  • Intrauterine Devices, Medicated
  • Levonorgestrel

Identity

PubMed Central ID

  • PMC4654647

Scopus Document Identifier

  • 84960485706

Digital Object Identifier (DOI)

  • 10.1016/j.contraception.2015.08.009

PubMed ID

  • 26297203

Additional Document Info

volume

  • 92

issue

  • 6