Clinical efficiency of a ready-to-use medium for human embryo culture supplemented with growth factors in patients with previous in vitro fertilization failures
Completed
- Conditions
- Intracytoplasmic sperm injection (ICSI) and embryo culturePregnancy and Childbirth
- Registration Number
- ISRCTN94726536
- Lead Sponsor
- Gynepro S.R.L.
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Female
- Target Recruitment
- 500
Inclusion Criteria
1. Female patients with at least one previous unsuccessful IVF attempt, in which a clinical pregnancy was not established (including biochemical pregnancies or miscarriages)
2. Aged between 25 and 45
Exclusion Criteria
1. Women older than 45 years old
2. Patients with male partners with testicular spermatozoa or severe oligoastenoteratozoospermia (total sperm number less than 1,000,000 and sperm motility less than 5%)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Implantation rate (defined as the number of implanted embryos per number of transferred embryos) is measured 30 days after embryo transfer.
- Secondary Outcome Measures
Name Time Method Pregnancy rate (defined as the number of pregnancies per number of transferred embryos) is measured using ultrasound of gestational chamber 30 days after embryo transfer.