Progesterone on the Day of Ovulation Induction is Associated With Pregnancy Outcome
NCT ID: NCT01426152
Last Updated: 2011-08-31
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
2555 participants
OBSERVATIONAL
2006-01-31
2011-04-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Low level progesterone group (1)
Progesterone \< 1.50 ng/mL on day of ovulation induction
No interventions assigned to this group
Medium level progesterone group (2)
Progesterone 1.51-1.99 ng/mL on the day of ovulation induction
No interventions assigned to this group
High level progesterone group (3)
Progesterone \> 1.99 ng/mL on the day of ovulation induction
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* progesterone measured on the day of ovulation induction
* informed consent
Exclusion Criteria
18 Years
FEMALE
No
Sponsors
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Bollmann Bruckner Noss
OTHER
Responsible Party
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Principal Investigators
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Robert Ochsenkuehn, MD
Role: PRINCIPAL_INVESTIGATOR
Center for Reproductive Medicine
Locations
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Praxis Bollmann-Brückner-Noss
Munich, Bavaria, Germany
Countries
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References
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Ochsenkuhn R, Arzberger A, von Schonfeldt V, Gallwas J, Rogenhofer N, Crispin A, Thaler CJ, Noss U. Subtle progesterone rise on the day of human chorionic gonadotropin administration is associated with lower live birth rates in women undergoing assisted reproductive technology: a retrospective study with 2,555 fresh embryo transfers. Fertil Steril. 2012 Aug;98(2):347-54. doi: 10.1016/j.fertnstert.2012.04.041. Epub 2012 May 24.
Other Identifiers
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BBN
Identifier Type: OTHER
Identifier Source: secondary_id
Prog2006-2011
Identifier Type: -
Identifier Source: org_study_id