Contraception
Volume 81, Issue 6 , Pages 501-509, June 2010

Long-term efficacy and safety of a monophasic combined oral contraceptive containing 0.02 mg ethinylestradiol and 2 mg chlormadinone acetate administered in a 24/4-day regimen

  • Cosima Brucker

      Affiliations

    • Klinikum Nürnberg Nord, Klinik für Frauenheilkunde, Prof.-Ernst-Nathan-Str. 1, 90419 Nürnberg, Germany
    • Corresponding Author InformationCorresponding author. Tel.: +49 911 3982222.
  • ,
  • Bernard Hedon

      Affiliations

    • Hôpital Arnaud de Villeneuve, 371, Av. Doyen Gaston Giraud, 34295 Montpellier Cedex 5, France
  • ,
  • Hok Sien The

      Affiliations

    • St. Antonius Ziekenhuis, Koekoekslaan 1, 3435 CM Nieuwegein, The Netherlands
  • ,
  • Kornelia Höschen

      Affiliations

    • Grünenthal GmbH, 52099 Aachen, Germany
  • ,
  • Natascha Binder

      Affiliations

    • Grünenthal GmbH, 52099 Aachen, Germany
  • ,
  • Annette Christoph

      Affiliations

    • Grünenthal GmbH, 52099 Aachen, Germany

Received 16 September 2008; received in revised form 11 January 2010; accepted 13 January 2010. published online 22 February 2010.

Abstract 

Objective

This study was conducted to assess the long-term efficacy and safety of a low-dose monophasic combined oral contraceptive (COC) containing 0.02 mg ethinylestradiol (EE) and 2 mg chlormadinone acetate (CMA) in a novel regimen administered daily for 24 days followed by a 4-day placebo interval.

Study Design

In this multicenter, uncontrolled, Phase III trial, 1665 subjects took the COC 0.02 mg EE/2 mg CMA for up to 21 cycles. The overall Pearl Index was the primary end point; cycle control, safety, effect on acne and seborrhea, and changes in body weight and libido were secondary end points.

Results

Contraceptive efficacy was analyzed for 1653 subjects completing 21,495 cycles. Six pregnancies occurred during trial duration with one attributable to method failure. The overall Pearl Index for the first year of use was 0.33 (95% confidence interval, 0.09–0.85). The mean number of bleeding/spotting days during six 90-day reference periods (RPs) decreased from 17.0 (RP 1) to 11.7 (RP 6), and the number of bleeding episodes per RP decreased from 3.8 (RP 1) to 2.7 (RP 6). Among subjects who presented with acne at the baseline visit, a decrease of papules/pustules and comedones was observed during the course of the trial. The most common “at least possibly related” adverse events were headache, breast discomfort and nausea. The tolerability and well-being was reported as being excellent or good in the majority of trial subjects (84.6% and 80.2%, respectively).

Conclusions

The low-dose COC 0.02 mg EE/2 mg CMA administered daily for 24 days followed by a 4-day placebo interval provides high contraceptive efficacy combined with an adequate cycle control and safety profile, beneficial effects on acne, and is well tolerated.

Keywords: Oral contraception, Combined oral contraceptive, Chlormadinone acetate, Low-dose ethinylestradiol, 24/4-day regimen, Pearl Index, Cycle control, Antiandrogenic

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 Conflict of interest statement: Professor Brucker is a member of an advisory board on 0.02 mg EE/2 mg CMA sponsored by Grünenthal GmbH, Aachen, Germany.

PII: S0010-7824(10)00012-0

doi:10.1016/j.contraception.2010.01.011

Contraception
Volume 81, Issue 6 , Pages 501-509, June 2010