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NCT00954265 Clinical Trial

Pregnancy Rates in IVF After Ovulation Triggering With Recombinant or Urinary Human Chorionic Gonadotrophin (HCG)

Pregnancy Clinical Trial

Official title:
Phase III Study on the Effects of Recombinant HCG Ovulation Triggering on Stimulation, Embryonic and Pregnancy Parameters in an IVF Program

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT00954265
Other study ID # rec-HCG 002
Secondary ID
Status Active, not recruiting
Phase Phase 3
First received August 6, 2009
Last updated December 23, 2009
Start date August 2005
Est. completion date September 2010

Study information
Verified date August 2009
Source Universitair Ziekenhuis Brussel
Contact n/a
Is FDA regulated No
Health authority Belgium: Institutional Review Board
Study type Interventional

Clinical Trial Summary

To access whether the ovulation triggering with rec-HCG instead urinary-HCG has any impact on the blastulation rate and pregnancy rate of patients undergoing IVF treatment

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 130
Est. completion date September 2010
Est. primary completion date December 2007
Accepts healthy volunteers No
Gender Female
Age group 20 Years to 36 Years
Eligibility Inclusion Criteria:

- FSH<12,

- normal sperm,less than 36y,

- single blastocyst transfer

Exclusion Criteria:

- endometriosis stage 3&4,

- pco

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Intervention

Drug:
• 10000 IU urinary HCG
ovulation triggering
• 250 mcg recombinant HCG
ovulation triggering

Locations
Country Name City State
Belgium Centre for Reproductive Medicine, UZ Brussel Brussels Jette

Sponsors (2)
Lead Sponsor Collaborator
Universitair Ziekenhuis Brussel Merck Serono International SA

Country where clinical trial is conducted

Belgium, 

Outcome
Type Measure Description Time frame Safety issue
Primary blastulation rate on day-5 No
Secondary pregnancy rates, VEGF levels, OHSS rate 14 days after oocyte pick up No
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