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Supplementing Intracytoplasmic Sperm Injection Handling Medium With Latrunculin A (ICSI-LA)

Latrunculin A Supplementation to ICSI Handling Medium

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03678818
Enrollment
300
Registered
2018-09-20
Start date
2018-09-25
Completion date
2019-04-30
Last updated
2019-05-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Infertility

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

Interventions

OTHERMedium Supplemented with Latrunculin A

A medium with in-house supplementation of Latrunculin A to decrease oocyte degeneration after ICSI and improve the survival rate

Sponsors

Ibn Sina Hospital
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 42 Years
Healthy volunteers
No

Inclusion criteria

* ICSI participants

Exclusion criteria

\-

Design outcomes

Primary

MeasureTime frame
oocyte survival rate6 days of culture

Secondary

MeasureTime frame
Blastocyst formation rate6 days of culture
Blastocyst quality rate6 days of culture
fertilization rate6 days of culture
Implantation rate7 weeks
Ongoing pregnancy rate12 weeks
Clinical pregnancy ratethree months

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026