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临床试验/NCT01902264
NCT01902264已完成3 期

Prospective, Open-label, Single-center Clinical Study to Investigate the Red Blood Cell and Plasma Folate Concentrations During a 24-week Treatment Period With the Combination of Drospirenone 3 mg Plus Ethinyl Estradiol 0.02 mg Plus Levomefolate Calcium 0.451 mg in Mexican Women Seeking Contraception

Bayer0 个研究点目标入组 34 人开始时间: 2013年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
Bayer
入组人数
34
主要终点
Change in RBC folate concentration from baseline to Week 24

研究概览

简要总结

The objective of this study is to compare the red blood cell (RBC) and plasma concentrations of folate in subjects treated with drospirenone (DRSP)/ethinyl estradiol (EE) plus levomefolate calcium (L-5-MTHF) at 24 weeks with respect to basal determination.

Increased intake of folic acid (synthetic form of the naturally occurring B-vitamin) before and in the first few weeks of pregnancy has been shown to reduce certain types of birth defects. This is important for women who may become pregnant following discontinuation of oral contraception. Information about any side effects that may occur will also be collected.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Healthy, Mexican female subjects requesting contraception
  • Age >/=18 to </=45 years (inclusive); smokers must not be older than 30 years at the time of informed consent
  • Normal or clinically insignificant cervical smear not requiring further follow-up; a cervical smear has to be taken at the screening visit, or a normal result has to be documented within the previous 6 months. Human papilloma virus (HPV) testing in subjects with atypical squamous cells of undetermined significance (ASCUS) can be used as an adjunctive test. Subjects with ASCUS can be included if they are negative for high-risk HPV strains.

排除标准

  • Pregnancy or lactation (less than 6 months since delivery, abortion, or lactation before start of treatment)
  • Body mass index (BMI) >30 kg/m2
  • Hypersensitivity to any ingredient in the study drug
  • Any diseases or conditions that can compromise the function of body systems and could result in altered absorption, excessive accumulation, impaired metabolism, or altered excretion of the study medication
  • Any diseases or conditions that might interfere with the conduct of the study or the interpretation of the results
  • Any disease or condition that may worsen under hormonal treatment according to the assessment and opinion of the investigator.
  • Undiagnosed abnormal genital bleeding
  • Abuse of alcohol, drugs or medicine (eg, laxatives)
  • Any medication that could result in excessive accumulation, impaired metabolism, or altered excretion of the study drug

研究组 & 干预措施

EE20/DRSP/L-5-MTHF

Experimental

干预措施: EE20/DRSP/L-5-MTHF (Beyaz, BAY98-7071) (Drug)

结局指标

主要结局

Change in RBC folate concentration from baseline to Week 24

时间窗: Baseline and Week 24

Change in plasma folate concentration from baseline to Week 24

时间窗: Baseline and Week 24

次要结局

  • Plasma folate concentration(Different time points up to 32 weeks)
  • RBC folate concentration(Different time points up to 32 weeks)

研究者

发起方
Bayer
申办方类型
Industry
责任方
Sponsor

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