ClinicalTrials.Veeva

Menu

Supplementing Intracytoplasmic Sperm Injection Handling Medium With Cytochalasin B (ICSI-CB)

I

Ibn Sina Hospital

Status

Completed

Conditions

Infertility

Treatments

Other: Cytochalasin B use in ICSI handling medium

Study type

Interventional

Funder types

Other

Identifiers

NCT03663634
IbnSinaIVF-ICSI-CB

Details and patient eligibility

About

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,

Enrollment

987 patients

Sex

Female

Ages

18 to 40 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All ICSI candidates patients

Exclusion criteria

  • No exclusion

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

987 participants in 2 patient groups

Handling Medium Supplemented with Cytochalasin B
Experimental group
Treatment:
Other: Cytochalasin B use in ICSI handling medium
Handling Medium as it is.
No Intervention group

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems