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Endometrial Advancement After Rec or u-HCG Triggering

U

Universitair Ziekenhuis Brussel

Status and phase

Completed
Phase 4

Conditions

Infertility

Treatments

Drug: 10000 IU urinary HCG
Drug: 250 mcg recombinant HCG

Study type

Interventional

Funder types

Other
Industry

Identifiers

NCT00953628
recHCG001

Details and patient eligibility

About

The purpose of this study is to investigate any potential advantages of replacing human chorionic gonadotropin (uhCG) with recombinant human chorionic gonadotropin (recHCG) for final oocyte maturation with regard to Ovarian hyperstimulation syndrome (OHSS)pathophysiology, endometrium receptivity and embryo quality and clinical pregnancy.

Full description

Biopsies of endometrium were taken in different groups Pregnancy rates were compared among defferent groups

Enrollment

130 patients

Sex

Female

Ages

20 to 36 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Less than 36 years old
  • Male or tubal infertility
  • FSH<12 on day 3

Exclusion criteria

  • Endometriosis stage 3 & 4

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

130 participants in 2 patient groups

o Group A=uHCG ovul trig
Active Comparator group
Description:
HCG for triggering
Treatment:
Drug: 10000 IU urinary HCG
o Group B=recHCG ovul trig
Experimental group
Description:
recombinant HCG for triggering
Treatment:
Drug: 250 mcg recombinant HCG

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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