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Clinical trial

Multicenter, Open-label, Uncontrolled Study to Investigate the Efficacy and Safety of the Transdermal Contraceptive Patch Containing 0.55 mg Ethinyl Estradiol and 2.1 mg Gestodene (Material no. 80876395) in a 21-day Regimen for 13 Cycles in 1650 Healthy Female Subjects

NCT00914693 is registered in ClinicalTrials.gov with Bayer as lead sponsor.

NCT NCT00914693
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Registry record

As filed in ClinicalTrials.gov.

Title
Multicenter, Open-label, Uncontrolled Study to Investigate the Efficacy and Safety of the Transdermal Contraceptive Patch Containing 0.55 mg Ethinyl Estradiol and 2.1 mg Gestodene (Material no. 80876395) in a 21-day Regimen for 13 Cycles in 1650 Healthy Female Subjects
Lead sponsor
Bayer
Phase
Phase 3
Overall status
Completed
Start date
April 30, 2009
Completion date
September 30, 2011
Enrollment
1,694 (actual)
Sites
66

Conditions

As the registry lists them; a condition with its own page is linked.

contraception