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Genetic Screening and Assisted Oocyte Activation in Couples With Diminished/Aberrant Embryonic Development. (AOA)

Primary Purpose

Embryo, Embryo Disorder, Genetic Disease

Status
Completed
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
AOA
Genetic screening
Calcium pattern analysis
Sponsored by
University Hospital, Ghent
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Embryo focused on measuring AOA, embryo developmental problems, genetic screening, calcium pattern analysis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients with one or more previous ICSI cycles (UZ Gent) AND
  • patients with:
  • complete developmental arrest (no transfer), or
  • complete developmental delay (no morula/blastocyst on Day 5), or
  • significantly reduced blastocyst formation (≤15%)
  • willing and able to give informed consent

Exclusion Criteria:

  • patients which went for oocyte or sperm donation
  • patients with severe male infertility or low fertilization (<33%) after ICSI
  • cycles requiring surgical sperm recovery procedures

Sites / Locations

  • Ghent University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

AOA, genetic screening, calcium pattern

Arm Description

Clinical setting: Patients will undergo ICSI-AOA. Furthermore, patients will give a saliva sample to do genetic screening. Genes important during oocyte activation and embryo development will be investigated. Also, calcium pattern analysis of the patients' spermatozoa will be executed.

Outcomes

Primary Outcome Measures

Blastocyst rate
Blastocyst rate will be calculated and blastocyst will be scored. The best quality embryos will be transferred and/or frozen.

Secondary Outcome Measures

Pregnancy rate
The level of beta-hCG in serum will be checked 16 days after oocyte retrieval
Live birth rate
Pregnant women will be followed up. Live births will be recorded.

Full Information

First Posted
November 21, 2017
Last Updated
May 24, 2023
Sponsor
University Hospital, Ghent
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1. Study Identification

Unique Protocol Identification Number
NCT03354013
Brief Title
Genetic Screening and Assisted Oocyte Activation in Couples With Diminished/Aberrant Embryonic Development.
Acronym
AOA
Official Title
Genetic Screening and Investigating the Effect of Assisted Oocyte Activation in Couples With Diminished/Aberrant Embryonic Development.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Completed
Study Start Date
January 15, 2018 (Actual)
Primary Completion Date
January 31, 2021 (Actual)
Study Completion Date
September 9, 2022 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Ghent

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
This is an interventional comparative study at the Department of Reproductive Medicine at Ghent University Hospital. Patients with previous embryo developmental problems are eligible for the study. Patients will undergo an ICSI-AOA treatment and will also be screened for genes important in the oocyte activation and embryonic development process. Also, the calcium releasing pattern of the patients' spermatozoa will be investigated.
Detailed Description
Assisted Oocyte Activation (ICSI-AOA) will be the treatment for these patients to overcome their previous embryo developmental problems. This protocol artificially induces calcium rises in the oocyte, which mimics the natural oocyte activation process induced by the sperm factor PLCzeta. If 6 or more mature oocytes are collected at oocyte retrieval, 50%ICSI and 50% ICSI-AOA will be applied to all oocytes. The best embryo(s) will be transferred back. Rest embryo(s) will be vitrified for future cycles. Patients will be followed up. Furthermore, an additional sperm sample will be produced to investigate the calcium inducing pattern of the patients' spermatozoa. Thereby, mouse and/or human (research-donated control oocytes) will be pre-incubated with a Ca2+ sensitive dye. Next, human spermatozoa will be injected into these mouse/human oocytes and the calcium pattern will be recorded under an inverted epifluorescence microscope. Both partners will give a saliva sample to screen for mutations possible genes involved in oocyte activation and embryo development.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Embryo, Embryo Disorder, Genetic Disease
Keywords
AOA, embryo developmental problems, genetic screening, calcium pattern analysis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
42 (Actual)

8. Arms, Groups, and Interventions

Arm Title
AOA, genetic screening, calcium pattern
Arm Type
Experimental
Arm Description
Clinical setting: Patients will undergo ICSI-AOA. Furthermore, patients will give a saliva sample to do genetic screening. Genes important during oocyte activation and embryo development will be investigated. Also, calcium pattern analysis of the patients' spermatozoa will be executed.
Intervention Type
Procedure
Intervention Name(s)
AOA
Intervention Description
100% ICSI-AOA will be performed.
Intervention Type
Diagnostic Test
Intervention Name(s)
Genetic screening
Intervention Description
Patients will donate a saliva sample. Genetic screening will take place for PLCzeta (male) and Dux4 (male and female). Also other possible genes involved in embryo development could be tested.
Intervention Type
Diagnostic Test
Intervention Name(s)
Calcium pattern analysis
Intervention Description
Male patients will donate a sperm sample. Calcium pattern analysis will take place by injecting the patients' sperm into mouse and/or human (in vitro matured) oocytes (research-donated control oocytes). This will estimate the sperm capability to induce calcium oscillations in the oocyte.
Primary Outcome Measure Information:
Title
Blastocyst rate
Description
Blastocyst rate will be calculated and blastocyst will be scored. The best quality embryos will be transferred and/or frozen.
Time Frame
5 days after oocyte retrieval
Secondary Outcome Measure Information:
Title
Pregnancy rate
Description
The level of beta-hCG in serum will be checked 16 days after oocyte retrieval
Time Frame
Positive hCG 16 days after oocyte retrieval
Title
Live birth rate
Description
Pregnant women will be followed up. Live births will be recorded.
Time Frame
37 - 42 weeks after last menstruation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients with one or more previous ICSI cycles (UZ Gent) AND patients with: complete developmental arrest (no transfer), or complete developmental delay (no morula/blastocyst on Day 5), or significantly reduced blastocyst formation (≤15%) willing and able to give informed consent Exclusion Criteria: patients which went for oocyte or sperm donation patients with severe male infertility or low fertilization (<33%) after ICSI cycles requiring surgical sperm recovery procedures
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Petra De Sutter, M.D; PhD
Organizational Affiliation
University Ghent
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Björn Heindryckx, Prof.; PhD
Organizational Affiliation
University Hospital, Ghent
Official's Role
Principal Investigator
Facility Information:
Facility Name
Ghent University Hospital
City
Ghent
State/Province
East-Flandres
ZIP/Postal Code
9000
Country
Belgium

12. IPD Sharing Statement

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Genetic Screening and Assisted Oocyte Activation in Couples With Diminished/Aberrant Embryonic Development.

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