Pregnancy Rates in IVF After Ovulation Triggering With Recombinant or Urinary Human Chorionic Gonadotrophin (HCG)
NCT ID: NCT00954265
Last Updated: 2009-12-24
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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UNKNOWN
PHASE3
130 participants
INTERVENTIONAL
2005-08-31
2010-09-30
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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RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
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Urinary-HCG group
These patients received u-HCG for ovulation triggering during ovarian stimulation for IVF
10000 IU urinary HCG
ovulation triggering
Recombinant HCG group
These patients received rec-HCG for ovulation triggering during ovarian stimulation for IVF
250 mcg recombinant HCG
ovulation triggering
Interventions
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10000 IU urinary HCG
ovulation triggering
250 mcg recombinant HCG
ovulation triggering
Eligibility Criteria
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Inclusion Criteria
* normal sperm,less than 36y,
* single blastocyst transfer
Exclusion Criteria
* pco
20 Years
36 Years
FEMALE
No
Sponsors
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Merck Serono International SA
INDUSTRY
Universitair Ziekenhuis Brussel
OTHER
Responsible Party
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Centre for Reproductive Medicine
Principal Investigators
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Paul Devroey, Professor
Role: STUDY_DIRECTOR
Professor or OB-GYN
Locations
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Centre for Reproductive Medicine, UZ Brussel
Brussels, Jette, Belgium
Countries
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Other Identifiers
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rec-HCG 002
Identifier Type: -
Identifier Source: org_study_id