Viewing Study NCT00185484



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Last Modification Date: 2024-10-26 @ 9:17 AM
Study NCT ID: NCT00185484
Status: COMPLETED
Last Update Posted: 2014-12-31
First Post: 2005-09-13

Brief Title: Efficacy and Safety Oral Contraceptive Study
Sponsor: Bayer
Organization: Bayer

Study Overview

Official Title: Multi-center Open Uncontrolled Study to Investigate the Efficacy and Safety of the Oral Contraceptive SH T 186 D Containing 002 mg Ethinylestradiol-b-cyclodextrin Clathrate and 3 mg Drospirenone in a 24-day Regimen for 13 Cycles in 1010 Healthy Female Volunteers
Status: COMPLETED
Status Verified Date: 2014-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to determine whether the study drug is effective in prevention of pregnancy in healthy women in reproductive age
Detailed Description: The study has previously been posted by Schering AG Germany Schering AG Germany has been renamed to Bayer Schering Pharma AG GermanyBayer Schering Pharma AG Germany is the sponsor of the trial

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None
Secondary IDs
Secondary ID Type Domain Link
308021 None None None