Microdose intrauterine levonorgestrel for contraception

1987 
Abstract An intrauterine device (IUD) releasing 2 μg of levonorgestrel per 24 hours was compared in a randomized multicentre clinical trial with two copper IUDs — the TCu 220C and the Nova T. The 2μg levonorgestrel device had statistically significantly higher pregnancy rates (from 390 days of use) and higher expulsion rates (up to 570 days). In addition, the total medical removals and removals for bleeding were significantly higher at all intervals where the data were analysed. Most disturbing was a 6.7 increased relative risk of ectopic pregnancy with the steroid-releasing IUD compared to the combined copper IUD data. It is concluded that the goal of microdose administration of 2μg levonorgestrel to the uterine cavity does not achieve the objectives of a new and improved IUD device which is safe and effective.
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