Contraception
Volume 63, Issue 6 , Pages 303-307, June 2001

A 12-month clinical investigation with a 24-day regimen containing 15 μg ethinylestradiol plus 60 μg gestodene with respect to hemostasis and cycle control

  • Franca Fruzzetti

      Affiliations

    • Department of Obstetrics and Gynecology, University of Pisa, Pisa, Italy
    • Corresponding Author InformationCorresponding author. Tel.: +39-50-992801; fax: +39-50-553910
  • ,
  • Andrea Riccardo Genazzani

      Affiliations

    • Department of Obstetrics and Gynecology, University of Pisa, Pisa, Italy
  • ,
  • Cabiria Ricci

      Affiliations

    • Department of Obstetrics and Gynecology, University of Pisa, Pisa, Italy
  • ,
  • Ferdinando De Negri

      Affiliations

    • Department of Internal Medicine, University of Pisa, Pisa, Italy
  • ,
  • Chiara Bersi

      Affiliations

    • Department of Obstetrics and Gynecology, University of Pisa, Pisa, Italy
  • ,
  • Franco Carmassi

      Affiliations

    • Department of Internal Medicine, University of Pisa, Pisa, Italy

Abstract 

The effects of a 24-day regimen containing 15 μg ethinyl estradiol (EE) plus 60 μg gestodene on cycle control and on hemostasis, were evaluated in 58 healthy women (age 19–47 years). All women received the pill for 12 months. Withdrawal bleeding at every cycle during the tablet-free interval was experienced by 84.5% of the women. The overall incidence of irregular bleedings was 19.3%. Hemostasis was evaluated in 20 women. No changes in plasma fibrinogen concentrations, nor in prothrombin fragment F1+2 were observed. A slight increase in thrombin-antithrombin III complexes was observed after 6 and 12 months of oral contraceptive use. Antithrombin III activity significantly increased after one-year of pill intake. The concentrations of tissue plasminogen activator and plasminogen activator inhibitor, both antigen and activity, did not change. These results show that very low doses of EE, such as 15 μg, do not impair hemostasis in healthy females. However, the reduction for the EE dose is responsible of some of the effects on cycle control.

Keywords: Oral contraceptives, Gestodene, Cycle control, Hemostasis

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PII: S0010-7824(01)00213-X

Contraception
Volume 63, Issue 6 , Pages 303-307, June 2001