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Citation(s)

  •   Bhattacharya SM, Jha A
    Comparative study of the therapeutic effects of oral contraceptive pills containing desogestrel, cyproterone acetate, and drospirenone in patients with polycystic ovary syndrome. Fertil Steril. 2012 Oct;98(4):1053-9. doi: 10.1016/j
  •   Bitzer J, Römer T, Lopes da Silva Filho A
    The use of cyproterone acetate/ethinyl estradiol in hyperandrogenic skin symptoms - a review. Eur J Contracept Reprod Health Care. 2017 Jun;22(3):172-182. doi: 10.1080/13625187.2017.1317339. Epub 2017 Apr 27. Rev
  •   Elger W, Beier S, Pollow K, Garfield R, Shi SQ, Hillisch A
    Conception and pharmacodynamic profile of drospirenone. Steroids. 2003 Nov;68(10-13):891-905.
  •   Garcia R, Benet M, Arnau C, Cobo E
    Efficiency of the cross-over design: an empirical estimation. Stat Med. 2004 Dec 30;23(24):3773-80.
  •   Kuhnz W, Staks T, Jütting G
    Pharmacokinetics of cyproterone acetate and ethinylestradiol in 15 women who received a combination oral contraceptive during three treatment cycles. Contraception. 1993 Dec;48(6):557-75.
  •   Luque-Ramírez M, Alvarez-Blasco F, Botella-Carretero JI, Martínez-Bermejo E, Lasunción MA, Escobar-Morreale HF
    Comparison of ethinyl-estradiol plus cyproterone acetate versus metformin effects on classic metabolic cardiovascular risk factors in women wit
  •   Sedgwick P
    Bias in randomised controlled trials: comparison of crossover group and parallel group designs. BMJ. 2015 Aug 7;351:h4283. doi: 10.1136/bmj.h4283.
  •   Sedgwick P
    Randomised controlled trials: "within subject" versus "between subject" designs. BMJ. 2014 Oct 24;349:g6435. doi: 10.1136/bmj.g6435.
  •   Sedgwick P
    What is a crossover trial? BMJ. 2014 May 9;348:g3191. doi: 10.1136/bmj.g3191.
  •   Speck U, Wendt H, Schulze PE, Jentsch D
    Bio-availability and pharmacokinetics of cyproterone acetate-14C and ethinyloestradiol-3H after oral administration as a coated tablet (SH B 209 AB). Contraception. 1976 Aug;14(2):151-63.

Bioequivalence Study of 2 mg Cyproterone Acetate and 0.035 mg Ethinyl Estradiol in Indonesian Healthy Females

Details for clinical trial NCT04964193