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

Primary Purpose

Infertility

Status
Completed
Phase
Not Applicable
Locations
Egypt
Study Type
Interventional
Intervention
Medium Supplemented with Latrunculin A
Sponsored by
Ibn Sina Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Infertility

Eligibility Criteria

18 Years - 42 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • ICSI participants

Exclusion Criteria:

-

Sites / Locations

  • Banon Assiut
  • IbnSina IVF Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Handling Medium Supplemented with Latrunculin A

Handling Medium as it is.

Arm Description

Outcomes

Primary Outcome Measures

oocyte survival rate

Secondary Outcome Measures

fertilization rate
Blastocyst formation rate
Blastocyst quality rate
Clinical pregnancy rate
Implantation rate
Ongoing pregnancy rate

Full Information

First Posted
September 17, 2018
Last Updated
May 5, 2019
Sponsor
Ibn Sina Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03678818
Brief Title
Supplementing Intracytoplasmic Sperm Injection Handling Medium With Latrunculin A (ICSI-LA)
Official Title
Latrunculin A 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 20, 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. 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,

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 Latrunculin A
Arm Type
Experimental
Arm Title
Handling Medium as it is.
Arm Type
No Intervention
Intervention Type
Other
Intervention Name(s)
Medium Supplemented with Latrunculin A
Intervention Description
A medium with in-house supplementation of Latrunculin A 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
Blastocyst quality 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 participants Exclusion Criteria: -
Facility Information:
Facility Name
Banon Assiut
City
Assiut
Country
Egypt
Facility Name
IbnSina IVF Center
City
Sohag
Country
Egypt

12. IPD Sharing Statement

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

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