Predictive Factors for Ovarian Stimulation Using a Fixed Daily Dose of 200 IU Recombinant FSH (Study 142003)(COMPLETED)(P05696) - Study Results

Predictive Factors for Ovarian Stimulation Using a Fixed Daily Dose of 200 IU Recombinant FSH (Study 142003)(COMPLETED)(P05696) (Xpect)

This study has been completed.

Study NCT00778999 Information provided by Schering-Plough

First Received: October 23, 2008 Last Updated: October 2, 2009 History of Changes

Study Type:	Interventional
Study Design:	Randomized, Open Label, Active Control, Parallel Assignment
Condition:	Infertility
Intervention:	Drug: Desogen/Marvelon

Participant Flow

Recruitment Details

Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
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Pre-Assignment Details

Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
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Reporting Groups

	Description
Desogen Oral Contraceptive	Use of oral contraceptive pills prior to controlled ovarian stimulation
Non-Oral Contraceptive	No use of oral contraceptive pills prior to controlled ovarian stimulation

Participant Flow: Overall Study

	Desogen Oral Contraceptive	Non-Oral Contraceptive
STARTED	223	219
COMPLETED	195	185
NOT COMPLETED	28	34
Discontinuation: no embryo transfer	14	14
Did not receive recFSH	14	20

Baseline Characteristics

Reporting Groups

	Description
Desogen Oral Contraceptive	Use of oral contraceptive pills prior to controlled ovarian stimulation
Non-Oral Contraceptive	No use of oral contraceptive pills prior to controlled ovarian stimulation

Baseline Measures

	Desogen Oral Contraceptive	Non-Oral Contraceptive	Total
Number of Participants [units: participants]	223	219	442
Age [units: participants]
<=18 years	0	0	0
Between 18 and 65 years	223	219	442
>=65 years	0	0	0
Gender [units: participants]
Female	223	219	442
Male	0	0	0