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Assessment of the Effectiveness and Tolerability of Ovarian Hyperstimulation — DESCARTES  

STERILITY Clinical Trial

Official title:
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

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

  • Ovarian Hyperstimulation Syndrome
  • STERILITY
Clinical Trial Details
NCT number NCT01331720
Study type Observational
Source Ferring Pharmaceuticals
Contact
Status Completed
Phase N/A
Start date November 2007
Completion date July 2010
View Details
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