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Efficacy and safety of a 28-day oral contraceptive with 7 days of low-dose estrogen in place of placebo.

机译:28天口服避孕药和7天低剂量雌激素代替安慰剂的疗效和安全性。

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BACKGROUND: The study was conducted to evaluate the efficacy and safety for the prevention of pregnancy of a 28-day oral contraceptive (OC) containing 150 mcg desogestrel (DSG)/20 mcg ethinyl estradiol (EE) for 21 days followed by 7 days of 10 mcg EE (Cette-28). STUDY DESIGN: A 6-month, prospective, multicenter, single-arm study was conducted in 1302 women aged 18-45 years. RESULTS: Over six cycles of treatment, the cumulative risk of pregnancy among all treated subjects (n=1262) was 0.9%. The Pearl Index for women 18-35 years of age (n=1042) was 2.20, including 9 pregnancies with estimated conception dates during active drug ingestion or up to 7 days after the last combination tablet. The rate of unscheduled bleeding was low and the duration of scheduled bleeding was approximately 2 days during each of the six treatment cycles. The safety profile was similar to what has been reported for other OCs. CONCLUSION: This low-dose, 28-day OC incorporating 7 days of 10 mcg EE during the hormone free interval is effective and safe for the prevention of pregnancy and is well-tolerated by women.
机译:背景:这项研究旨在评估预防妊娠28天,口服150毫克去氧孕烯(DSG)/ 20毫克乙炔雌二醇(EE)的28天口服避孕药(OC)的有效性和安全性。 10 mcg EE(Cette-28)。研究设计:对1302名年龄在18-45岁的女性进行了为期6个月的前瞻性多中心单臂研究。结果:在六个治疗周期中,所有接受治疗的受试者(n = 1262)的累积妊娠风险为0.9%。 18-35岁(n = 1042)的女性的Pearl指数为2.20,其中包括9例妊娠,估计在服药期间或最后一次合用片剂后7天以内受孕。在六个治疗周期的每个周期中,计划外出血的发生率较低,计划内出血的持续时间约为2天。安全性与其他OC相似。结论:这种低剂量,28天的口服避孕药在无激素间隔期间结合7天的10 mcg EE是有效且安全的,可预防妊娠,并且女性耐受性良好。

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