Clinical Trials Directory

Trials / Unknown

UnknownNCT00415766

Comparison Between Recombinant Versus Urinary hCG for Ovulation Induction in High Responders

Recombinant hCG (Ovitrelle) Vesrus Urinary hCG (Pregnyl) for Triggering Final Oocyte Maturation in High Responders

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
150 (actual)
Sponsor
Eugonia · Academic / Other
Sex
Female
Age
18 Years – 39 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to compare the clinical outcomes of recombinant human chorionic gonadotrophin (rHCG) and urinary HCG (uHCG) in patients undergoing IVF cycles.

Detailed description

Urinary human chorionic gonadotrophin (u-hCG) has been widely used to induce final oocyte maturation and to trigger ovulation in assisted conception. Recombinant technology has allowed the production of r-hCG inj which all urinary contaminants are absent. Hence, this would allow the safe subcutaneous administration of a compound with less batch-to-batch variation. This study will investigate the effectiveness of the recombinant hCG compared to the currently used urinary hCG.

Conditions

Interventions

TypeNameDescription
DRUGrHCG 250ugInjection of 250 ug Ovitrelle to trigger final oocyte maturation
DRUGuHCG 5000 IUInjection of 5000 IU Pregnyl to trigger final oocyte maturation
DRUGuHCG 7500 IUInjection of 7500 IU Pregnyl to trigger final oocyte maturation

Timeline

Start date
2013-06-01
Primary completion
2015-12-01
Completion
2016-07-01
First posted
2006-12-25
Last updated
2016-01-20

Locations

1 site across 1 country: Greece

Source: ClinicalTrials.gov record NCT00415766. Inclusion in this directory is not an endorsement.