- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03678558
Oocyte Vitrification Aided With Cytochalasin B
August 5, 2019 updated by: Muhammad Fawzy, Ibn Sina Hospital
Cytochalasin B for Oocyte Vitrification
Using the cytoskeleton Stabilizer the Cytochalasin B would improve the outcome of oocyte vitrification.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
612
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
-
Sohag, Egypt, 12345
- IbnSina IVF Center, IbnSina Hospital
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 42 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- indication for oocyte vitrification
Exclusion Criteria:
-
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Other
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: Vitrification medium with no supplementation
|
|
Experimental: Cytochalasin B supplemented vitrification medium
|
Vitrification of human oocyte in medium supplemented with Cytochalasin B
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
survival after thawing
Time Frame: 6 days of culture
|
6 days of culture
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
fertilization rate
Time Frame: 6 days of culture
|
6 days of culture
|
|
ongoing pregnancy rate
Time Frame: 12 months
|
12 months
|
|
clinical pregnancy rate
Time Frame: three months
|
three months
|
|
Rates of blastocyst formation and quality
Time Frame: 6 days of culture
|
Number of formed blastocyst and blastocyst with high-quality per fertilized oocytes
|
6 days of culture
|
embryo utilisation rate
Time Frame: 6 days of culture
|
6 days of culture
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
September 25, 2018
Primary Completion (Actual)
August 5, 2019
Study Completion (Actual)
August 5, 2019
Study Registration Dates
First Submitted
September 17, 2018
First Submitted That Met QC Criteria
September 18, 2018
First Posted (Actual)
September 19, 2018
Study Record Updates
Last Update Posted (Actual)
August 7, 2019
Last Update Submitted That Met QC Criteria
August 5, 2019
Last Verified
August 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- IbnSina-Oocyte-CB
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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