Multinational, multicentre, randomised, open-label study evaluating the impact of a 91-day extended regimen combined oral contraceptive, compared with two 28-day traditional combined oral contraceptives, on haemostatic parameters in healthy women

Eur J Contracept Reprod Health Care. 2014 Aug;19(4):285-94. doi: 10.3109/13625187.2014.918596. Epub 2014 Jun 13.

Abstract

Objectives: To evaluate the impact of a 91-day extended regimen combined oral contraceptive (150 μg levonorgestrel [LNG]/30 μg ethinylestradiol [EE] for 84 days, followed by 10 μg EE for seven days [Treatment 1]) compared with two traditional 21/7 regimens (21 days 150 μg LNG/30 μg EE [Treatment 2] or 150 μg desogestrel [DSG]/30 μg EE [Treatment 3], both with seven days' hormone free), on several coagulation factors and thrombin formation markers.

Methods: Randomised, open-label, parallel-group comparative study involving healthy women (18-40 years). The primary endpoint was change from baseline in prothrombin fragment 1 + 2 (F1 + 2) levels over six months.

Results: A total of 187 subjects were included in the primary analysis. In all groups, mean F1 + 2 values were elevated after six months of treatment. Changes were comparable between Treatments 1 and 2 (least squares mean change: 170 pmol/L and 158 pmol/L, respectively) but noticeably larger after Treatment 3 (least squares mean change: 592 pmol/L). The haemostatic effects of Treatment 1 were comparable to those of Treatment 2 and noninferior to those of Treatment 3 (lower limit of 95% confidence interval [- 18.3 pmol/L] > - 130 pmol/L).

Conclusions: The LNG/EE regimens had similar effects on F1 + 2. Noninferiority was demonstrated between extended regimen LNG/EE and DSG/EE.

Keywords: Coagulation; Combined oral contraceptives; Desogestrel; Haemostatic; Levonorgestrel.

Publication types

  • Comparative Study
  • Multicenter Study
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Blood Coagulation / drug effects*
  • Contraceptives, Oral, Combined / adverse effects
  • Contraceptives, Oral, Combined / pharmacology
  • Contraceptives, Oral, Combined / therapeutic use*
  • Delayed-Action Preparations / adverse effects
  • Delayed-Action Preparations / therapeutic use
  • Desogestrel / administration & dosage
  • Desogestrel / adverse effects
  • Desogestrel / therapeutic use
  • Drug Administration Schedule
  • Ethinyl Estradiol / administration & dosage
  • Ethinyl Estradiol / adverse effects
  • Ethinyl Estradiol / pharmacology
  • Ethinyl Estradiol / therapeutic use
  • Factor VII / analysis
  • Factor VIII / analysis
  • Female
  • Fibrin Fibrinogen Degradation Products / analysis
  • Humans
  • Levonorgestrel / administration & dosage
  • Levonorgestrel / adverse effects
  • Levonorgestrel / pharmacology
  • Levonorgestrel / therapeutic use
  • Partial Thromboplastin Time
  • Prothrombin / analysis
  • Young Adult

Substances

  • Contraceptives, Oral, Combined
  • Delayed-Action Preparations
  • Fibrin Fibrinogen Degradation Products
  • fibrin fragment D
  • Ethinyl Estradiol
  • Levonorgestrel
  • Desogestrel
  • Factor VII
  • Prothrombin
  • Factor VIII