A dose finding study to assess contraceptive efficacy and the effect on liver function of estetrol contraception.
Completed
- Conditions
- Hormonal contraceptive method
- Registration Number
- NL-OMON27454
- Lead Sponsor
- Estetra S.A.mw. X.Y. Zimmermanp/a Postbus 4643700 AL ZeistTel: +31 30 6 985 020Fax: +31 30 6 985 021yz@pantarheibio.com
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
1. At least 18 years and not older than 35 years of age;
2. Willing to use a barrier method of contraception during wash-out;
Exclusion Criteria
1. Clinically significant abnormal results of routine haematology, serum biocemistry, urinalysis and/or ECG;
2. Women with a washout cycle with a duration of more than 42 days;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method