Oocyte Vitrification Aided With Cytochalasin B
Primary Purpose
Infertility
Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Cytochalasin B supplemented vitrification medium
Sponsored by
About this trial
This is an interventional other trial for Infertility
Eligibility Criteria
Inclusion Criteria:
- indication for oocyte vitrification
Exclusion Criteria:
-
Sites / Locations
- IbnSina IVF Center, IbnSina Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Cytochalasin B supplemented vitrification medium
Vitrification medium with no supplementation
Arm Description
Outcomes
Primary Outcome Measures
survival after thawing
Secondary Outcome Measures
fertilization rate
Rates of blastocyst formation and quality
Number of formed blastocyst and blastocyst with high-quality per fertilized oocytes
embryo utilisation rate
clinical pregnancy rate
ongoing pregnancy rate
Full Information
NCT ID
NCT03678558
First Posted
September 17, 2018
Last Updated
August 5, 2019
Sponsor
Ibn Sina Hospital
Collaborators
Banoon IVF Center
1. Study Identification
Unique Protocol Identification Number
NCT03678558
Brief Title
Oocyte Vitrification Aided With Cytochalasin B
Official Title
Cytochalasin B for Oocyte Vitrification
Study Type
Interventional
2. Study Status
Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
September 25, 2018 (Actual)
Primary Completion Date
August 5, 2019 (Actual)
Study Completion Date
August 5, 2019 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ibn Sina Hospital
Collaborators
Banoon IVF Center
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
Using the cytoskeleton Stabilizer the Cytochalasin B would improve the outcome of oocyte vitrification.
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
612 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Cytochalasin B supplemented vitrification medium
Arm Type
Experimental
Arm Title
Vitrification medium with no supplementation
Arm Type
No Intervention
Intervention Type
Other
Intervention Name(s)
Cytochalasin B supplemented vitrification medium
Intervention Description
Vitrification of human oocyte in medium supplemented with Cytochalasin B
Primary Outcome Measure Information:
Title
survival after thawing
Time Frame
6 days of culture
Secondary Outcome Measure Information:
Title
fertilization rate
Time Frame
6 days of culture
Title
Rates of blastocyst formation and quality
Description
Number of formed blastocyst and blastocyst with high-quality per fertilized oocytes
Time Frame
6 days of culture
Title
embryo utilisation rate
Time Frame
6 days of culture
Title
clinical pregnancy rate
Time Frame
three months
Title
ongoing pregnancy rate
Time Frame
12 months
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:
indication for oocyte vitrification
Exclusion Criteria:
-
Facility Information:
Facility Name
IbnSina IVF Center, IbnSina Hospital
City
Sohag
ZIP/Postal Code
12345
Country
Egypt
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Oocyte Vitrification Aided With Cytochalasin B
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