跳至主要内容
临床试验/EUCTR2010-019902-17-GB
EUCTR2010-019902-17-GB进行中(未招募)不适用

A multicenter, open-label, randomized, controlled, two-arm study to assess compliance with daily tablet intake of women on treatment with the oral contraceptive SH T00186D/BAY 86-5300 (0.02 mg ethinyl estradiol as betadex clathrate and 3 mg drospirenone) in a flexible extended regimen supported by a dispenser (CADDY) with a reminder function over 12 months - EU-Compliance by buzzer study of YAZ Flex in the CADDY

Bayer HealthCare AG0 个研究点目标入组 500 人开始时间: 2010年10月26日最近更新:
相关药物

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
500

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
Female

入选标准

  • 1)Signed and dated informed consent
  • 2)Healthy female subjects requesting contraception
  • 3)Age between 18 and 35 years (inclusive), smokers must not be older than 30 years at the time point of informed consent
  • 4)Normal or clinically insignificant cervical smear not requiring further follow up (a cervical smear has to be taken at screening visit or a normal result has to be documented within the previous 6 months). Subjects with ASCUS can be included if they are negative for high-risk HPV strains. (HPV testing in subjects with ASCUS will be used as an adjunctive test).
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 500
  • F.1.3 Elderly (>=65 years) no
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - Pregnancy or lactation (less than 3 months since delivery, abortion, or lactation before start of treatment)
  • - Body mass index (BMI) >=30.0 kg/m2
  • - Presence or a history of venous or arterial thrombotic/thromboembolic events
  • - Repeated measurements of systolic blood pressure > 140 mmHg and/or diastolic blood pressure > 90 mmHg.
  • - Presence or history of liver tumors (benign or malignant), severe hepatic disease, jaundice and/or pruritus related to cholestasis, cholestatic jaundice associated with pregnancy or previous COC use
  • - Uncontrolled diabetes mellitus and/or diabetes mellitus with vascular involvement
  • - Severe dyslipoproteinemia
  • - Malignant or premalignant disease
  • - Uncontrolled thyroid disorder
  • - Chronic inflammatory bowel disease
  • - Severe renal insufficiency or acute renal failure
  • - History of migraine with focal neurologic symptoms
  • - Epilepsy

研究者

相似试验

进行中(未招募)
不适用
A multicenter, open-label, randomized, controlled, two-arm study to assess compliance with daily tablet intake of women on treatment with the oral contraceptive SH T00186D/BAY 86-5300 (0.02 mg ethinyl estradiol as betadex clathrate and 3 mg drospirenone) in a flexible extended regimen supported by a dispenser (CADDY) with a reminder function over 12 months - EU-Compliance by buzzer study of YAZ Flex in the CADDYContraceptionMedDRA version: 12.1Level: LLTClassification code 10030970Term: Oral contraception
EUCTR2010-019902-17-DEBayer HealthCare AG500
进行中(未招募)
不适用
A multicenter, open-label, randomized, controlled, two-arm study to assess compliance with daily tablet intake of women on treatment with the oral contraceptive SH T00186D/BAY 86-5300 (0.02 mg ethinyl estradiol as betadex clathrate and 3 mg drospirenone) in a flexible extended regimen supported by a dispenser (CADDY) with a reminder function over 12 months - EU-Compliance by buzzer study of YAZ Flex in the CADDYContraceptionMedDRA version: 9.1Level: PTClassification code 10030970
EUCTR2010-019902-17-ITBayer HealthCare AG500
进行中(未招募)
1 期
Phase 3, open-label study of ALXN1840 versus standard of care in pediatric participants with Wilson diseaseWilson DiseaseMedDRA version: 20.0Level: LLTClassification code 10047988Term: Wilson's diseaseSystem Organ Class: 100000004850
EUCTR2021-001015-82-PLAlexion Pharmaceuticals, Inc.48
进行中(未招募)
3 期
Phase 3, open-label study of ALXN1840 versus standard of care in pediatric participants with Wilson diseaseWilson disease
JPRN-jRCT2011210038Kobayashi Hiroshi48
进行中(未招募)
1 期
Phase 3, open-label study of ALXN1840 versus standard of care in pediatric participants with Wilson disease
EUCTR2021-001015-82-ESAlexion Pharmaceuticals, Inc.48