Back to resultsSupplementing Intracytoplasmic Sperm Injection Handling Medium With Cytochalasin D ( ICSI-CD)
Primary Purpose
Infertility
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Medium Supplemented with Cytochalasin D
Sponsored by
About this trial
This is an interventional other trial for Infertility
Eligibility Criteria
Inclusion Criteria:
- ICSI indicated participants
Exclusion Criteria:
-
Sites / Locations
- Banon Assiut
- IbnSina IVF Center, IbnSina Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Handling Medium Supplemented with Cytochalasin D
Handling Medium as it is.
Arm Description
Outcomes
Primary Outcome Measures
Oocyte survival rate
Secondary Outcome Measures
Fertilization rate
Blastocyst formation rate
Embryo utilization rate
Clinical pregnancy rate
Implantation rate
Ongoing pregnancy rate
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT03677492
Brief Title
Supplementing Intracytoplasmic Sperm Injection Handling Medium With Cytochalasin D ( ICSI-CD)
Official Title
Cytochalasin D Supplementation to ICSI Handling Medium
Study Type
Interventional
2. Study Status
Record Verification Date
May 2019
Overall Recruitment Status
Completed
Study Start Date
September 25, 2018 (Actual)
Primary Completion Date
April 25, 2019 (Actual)
Study Completion Date
April 30, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ibn Sina Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
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. 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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility
7. Study Design
Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Randomized
Enrollment
300 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Handling Medium Supplemented with Cytochalasin D
Arm Type
Experimental
Arm Title
Handling Medium as it is.
Arm Type
No Intervention
Intervention Type
Other
Intervention Name(s)
Medium Supplemented with Cytochalasin D
Intervention Description
A medium with in-house supplementation of Cytochalasin D to decrease oocyte degeneration after ICSI and improve the survival rate
Primary Outcome Measure Information:
Title
Oocyte survival rate
Time Frame
6 days of culture
Secondary Outcome Measure Information:
Title
Fertilization rate
Time Frame
6 days of culture
Title
Blastocyst formation rate
Time Frame
6 days of culture
Title
Embryo utilization rate
Time Frame
6 days of culture
Title
Clinical pregnancy rate
Time Frame
three months
Title
Implantation rate
Time Frame
7 weeks
Title
Ongoing pregnancy rate
Time Frame
12 weeks
10. Eligibility
Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
42 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
ICSI indicated participants
Exclusion Criteria:
-
Facility Information:
Facility Name
Banon Assiut
City
Assiut
Country
Egypt
Facility Name
IbnSina IVF Center, IbnSina Hospital
City
Sohag
ZIP/Postal Code
12345
Country
Egypt
12. IPD Sharing Statement
Learn more about this trial
Supplementing Intracytoplasmic Sperm Injection Handling Medium With Cytochalasin D ( ICSI-CD)
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