Postcoital estrogen or IUD?

In: Planned Parenthood in Europe regional information bulletin = Planning familial en Europe bulletin d'information regional = Familienplanung in Europe regionale informationen · 1979 · vol. 8(3) , pp. 7–8 · PMID:12178344 · W2425971987
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Abstract

In 1977-78, 120 women aged 15-35 at the CEMP Centre in Milan, Italy, were assigned randomly (60 each) to 5 tablets EE (1 mg) daily for 5 days; or insertion of Cu-T. All women were followed up for at least 40 days from last menstrual period. 88% were nulliparous; 90% were under age 25. With ovulation estimated as 14 days before the mean length of the 6 previous cycles, 40% had had unprotected coitus within 2 days of ovulation; 30% had coitus 3-4 days before or 3-5 days after ovulation. None of the 120 women became pregnant. Of the 60 women taking EE, 80% experienced side effects; 51% nausea, 18% vomiting; 30% breast pain; 25% headache, and 22% bleeding. The side effects from the Cu-T were 38%: 8% vagal reflex during insertion; 11% serious uterine cramps within 4 days of insertion; 33% bleeding; and 1 expelled 5 days after insertion. Both postcoital ethinylestradiol and the Copper-T 200 were effective in preventing pregnancy.

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