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Effect of Ca2+ Ionophore on Embryonic Development and Clinical Outcome in Cases With Previous Fertilization Arrest

A Prospective Randomized Controlled Trial Investigating Embryonic Development and Clinical Outcome After Using Ca2+ Ionophore in Cases With Previous Fertilization Arrest

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02683031
Enrollment
50
Registered
2016-02-17
Start date
2014-05-31
Completion date
2017-12-31
Last updated
2016-08-18

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

Conditions

Fertilization Arrest

Keywords

fertilization arrest, Cleavage failure, Embryonic development, Calcium ionophore

Brief summary

We aimed to investigate the efficiency of chemical oocyte activation using readymade Ca2+ ionophore on cases with previously cancelled cases due to fertilization arrest at pronuclear stage i.e: cleavage failure to find out if there is any improvement in embryonic developmental stages.

Detailed description

Many studies reported that Ca2+ ionophore has a positive effect on embryo development in cases with complete or partial fertilization failure. However, only one preliminary report suggested a beneficial effect of Ca2+ ionophore activation in four cases with fertilization arrest.

Interventions

OTHERCa2+ ionophore

Ca2+ ionophore is a chemical agent used to perform oocyte activation after ICSI. It showed effective treatment to get better fertilization, pregnancy, and healthy livebirth in cases with total or partial fertilization failure.

Sponsors

Benha University
CollaboratorOTHER
TopLab Company for ART Laboratories Consultation and Training
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
20 Years to 39 Years
Healthy volunteers
No

Inclusion criteria

* Patients with previous history of complete fertilization arrest. * ovarian stimulation with the GnRH agonist and recombinant FSH in a long protocol.

Exclusion criteria

* Female age \>40 years

Design outcomes

Primary

MeasureTime frameDescription
Blastocyst formation rate5 to 7days post oocyte retrivalDefined as the total number of blastocyst / total number of cleaved Embryos

Countries

Egypt

Contacts

Primary ContactYasmin Magdi, M.Sc
Yas.magdi@hotmail.com+201282313979
Backup ContactAhmed El-Damen, M.Sc
Ahmed_eldamen@Yahoo.com+201002414342

Outcome results

None listed

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