Trials / Completed
CompletedNCT01331720
Assessment of the Effectiveness and Tolerability of Ovarian Hyperstimulation
Assessment of the Effectiveness and Tolerability of Ovarian Hyperstimulation Protocols Which Are the Most Common in Clinical Practice Using High Purified Gonadotrophins (u-FSH-HP y u-hMG-HP) in IVF/ICSI
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 279 (actual)
- Sponsor
- Ferring Pharmaceuticals · Industry
- Sex
- Female
- Age
- —
- Healthy volunteers
- Not accepted
Summary
The aim of the study is to assess the effectiveness of 5 mixed protocols of ovarian hyperstimulation with urinary gonadotrophins to achieve clinical pregnancy in females undergoing assisted reproductive techniques (IVF/ICSI) (in-vitro fertilisation/intracytoplasmic sperm injection). Study hypothesis: mixed protocols with urinary FSH (follicle-stimulating hormone) and urinary hMG (human menopausal gonadotropin)should be more effective than monotherapy.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | hMG-HP |
Timeline
- Start date
- 2007-11-01
- Primary completion
- 2009-03-01
- Completion
- 2010-07-01
- First posted
- 2011-04-08
- Last updated
- 2011-04-08
Locations
14 sites across 1 country: Spain
Source: ClinicalTrials.gov record NCT01331720. Inclusion in this directory is not an endorsement.