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
| Type | Name | Description |
|---|---|---|
| DRUG | rHCG 250ug | Injection of 250 ug Ovitrelle to trigger final oocyte maturation |
| DRUG | uHCG 5000 IU | Injection of 5000 IU Pregnyl to trigger final oocyte maturation |
| DRUG | uHCG 7500 IU | Injection 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.