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CompletedNCT03663634

Supplementing Intracytoplasmic Sperm Injection Handling Medium With Cytochalasin B

Cytochalasin B Supplementation to ICSI Handling Medium

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
987 (actual)
Sponsor
Ibn Sina Hospital · Other Government
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Vienna Consensus has identified 10% damage rate after ICSI as a competency value. Despite the highest quality embryologists doing ICSI, degeneration sometimes occurs due to oocyte factors such as the fragile membrane, etc. Cytochalasin B serves to facilitate spindle or pronuclear transfer procedures helping to reduce the damage rate with no harm reported. Using Cytochalasin B during ICSI could serve to rescue some oocytes from the degeneration allowing for more chances of viable zygotes,

Conditions

Interventions

TypeNameDescription
OTHERCytochalasin B use in ICSI handling mediumA medium with in-house supplementation of Cytochalasin B to decrease oocyte degeneration after ICSI and improve survival rate

Timeline

Start date
2018-09-16
Primary completion
2019-07-20
Completion
2019-08-01
First posted
2018-09-10
Last updated
2019-08-07

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03663634. Inclusion in this directory is not an endorsement.

Supplementing Intracytoplasmic Sperm Injection Handling Medium With Cytochalasin B (NCT03663634) · Clinical Trials Directory