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Comparison of two ready-to-use systems specially designed for physiological intracytoplasmic sperm injection (ICSI): PICSI® versus Sperm Slow™, a prospective randomised trial

Not Applicable
Completed
Conditions
Intracytoplasmic sperm injection (ICSI)
Pregnancy and Childbirth
Fertility
Registration Number
ISRCTN72668039
Lead Sponsor
GynePro Medical Centers (Italy)
Brief Summary

2012 results in https://pubmed.ncbi.nlm.nih.gov/22749221/ (added 18/12/2020)

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
100
Inclusion Criteria

1. Infertile women not older than 41 years undergoing ICSI treatment at GynePro Medical Center
2. Semen parameters of the male partner:
2.1. Presence of ejaculate motile spermatozoa with total sperm number greater than or equal to 1,000,000
2.2. Sperm motility greater than or equal to 5%

Exclusion Criteria

1. Women older than 41 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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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