Clinical Trial Results:
A Multinational, Multicenter, Randomized, Open-Label Study to Evaluate the Impact of a 91-day Extended Cycle Oral Contraceptive Regimen, Compared to two 28-day Standard Oral Contraceptive Regimens, on Hemostatic Parameters in Healthy Women
Summary
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EudraCT number |
2010-023215-34 |
Trial protocol |
IT |
Global completion date |
02 Dec 2011
|
Paediatric regulatory details
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Is the trial part of an agreed EMA paediatric investigation plan? |
No
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Is the trial in scope of article 45 of Regulation (EC) No 1901/2006? |
No
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Is the trial in scope of article 46 of Regulation (EC) No 1901/2006? |
No
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Results information
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Results version number |
v1(current) |
This version publication date |
03 Nov 2018
|
First version publication date |
03 Nov 2018
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Other versions |
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Summary report(s) |
PSE-HSP-203 CT.gov PRS_Receipt Redacted.pdf |
Note: The legislation allows summary attachments to be posted instead of the full dataset for this trial. Refer to Commission Guideline 2012/C 302/03
for further information.