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Supplementing Intracytoplasmic Sperm Injection Handling Medium With Cytochalasin D ( ICSI-CD)

Infertility Clinical Trial

Official title:
Cytochalasin D Supplementation to ICSI Handling Medium

Clinical Trial 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 D serves to facilitate spindle or pronuclear transfer procedures helping to reduce the damage rate with no harm reported. Using Cytochalasin D during ICSI could serve to rescue some oocytes from the degeneration allowing for more chances of viable zygotes.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03677492
Study type Interventional
Source Ibn Sina Hospital
Contact
Status Completed
Phase N/A
Start date September 25, 2018
Completion date April 30, 2019
View Details
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