search
Back to results

AOA in Recurrent Fertilization Failure (AOA)

Primary Purpose

Infertility Primary

Status
Completed
Phase
Phase 4
Locations
Egypt
Study Type
Interventional
Intervention
Calcium Ionophore A23187
Sponsored by
MOHAMED BEHERY
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility Primary

Eligibility Criteria

20 Years - 40 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • (1) Age between 20 and 40 years old. (2) Cases with history of total fertilization failure in previous ICSI cycles (3) Oocytes with normal morphology.

Exclusion Criteria:

  • (1) Abnormal oocyte morphology degenerated or immature oocytes. (2) Husbands with spermatogenic arrest or Sertoli/Leydig cells only.

Sites / Locations

  • Al-Azhar University

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

No Intervention

Arm Label

study group

control group

Arm Description

. This group involved 75 patients with history of fertilization failure in which oocytes were activated by calcium ionophores

This group involved 75 patients with history of fertilization failure in which oocytes were not activated by calcium ionophores

Outcomes

Primary Outcome Measures

fertilization rate
the number of reproduced embryos divided by the number of fertilized oocytes

Secondary Outcome Measures

Pregnancy rate
the number of clinically pregnant women divided by the number of total patients undergoing ICSI procedures in the same group

Full Information

First Posted
February 4, 2021
Last Updated
February 4, 2021
Sponsor
MOHAMED BEHERY
search

1. Study Identification

Unique Protocol Identification Number
NCT04744753
Brief Title
AOA in Recurrent Fertilization Failure
Acronym
AOA
Official Title
Assisted Oocyte Activation (AOA) in Recurrent Fertilization Failure
Study Type
Interventional

2. Study Status

Record Verification Date
February 2021
Overall Recruitment Status
Completed
Study Start Date
July 15, 2017 (Actual)
Primary Completion Date
November 1, 2018 (Actual)
Study Completion Date
November 17, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
MOHAMED BEHERY

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Background: Despite the high success rate of ICSI, total fertilization failure still occurs in 1-3% of all ICSI cycles and can recur in subsequent cycles, even when a sufficient number of oocytes and motile spermatozoa are available. Several reports show that the majority of couples suffering from ICSI failure benefit from the application of ICSI combined with assisted oocyte activation. A variety of artificial activating methods is used in human assisted reproduction treatment, including physical, mechanical or chemical stimuli, which provoke one or more calcium rises in the oocyte cytoplasm. Study Design: Randomized controlled trial. Setting: A university fertility center. Methods: 150 infertile patients who underwent ICSI and all had history of recurrent fertilization failure. The patients were randomly allocated into 2 equal groups. Group1=75 patients who underwent ICSI without oocyte activation. Group2 patients =75 and underwent ICSI Patient underwent ICSI with oocyte activation. Reproductive outcomes were compared between both groups. Results: there were significant differences between groups regarding number of oocytes retrieved, number of mature oocyte, fertilization rate and pregnancy rate. Conclusion: Assisted oocyte activation with calcium ionophore results in significant improvement in the fertilization, cleavage and pregnancy rates after ICSI.
Detailed Description
This study is a randomized controlled trial included 150 ICSI patients with history of recurrent fertilization failure. Patients had undergone ICSI trials in ART unit, Al-Azhar University, Cairo, Egypt, from July 2017 to November 2018. The study was approved by the university medical ethical committee (under registry number 202010454) and all couples had signed a written consent before initiation of the study and the treatment cycles. AOA candidate couples were counseled regarding the procedure. The patients were selected according to the following criteria: Inclusion Criteria: - Age between 20 and 40 years old. Cases with history of total fertilization failure in previous ICSI cycles Oocytes with normal morphology. Male factor infertility. Exclusion Criteria: - Abnormal oocyte morphology degenerated or immature oocytes. Two groups were randomly designated: The first Group: The oocytes were treated by calcium ionophore. This group involved 75 ICSI cycles. The Second Group: Oocytes were not treated by calcium ionophore. This group involved 75 ICSI cycles. Methods: Ovarian stimulation: All women received ovarian stimulating drugs according to the ART protocols (long agonist, flare up or antagonist protocols). Deca 0.1 was given s.c. daily, for down-regulation in short and long protocol while cetrotide 0.25 was given s.c. daily for down-regulation in antagonist protocol. Follicular development was monitored by ultrasound scanning and serum estradiol. Patients received 10,000 IU of Human Chronic Gonadotrophin (HCG) when most of the follicles measured more than 17-20 mm in diameter. Semen preparation: • The husband was asked to submit a semen sample in a sterile plastic container after a 2 to 3-day period of abstinence and about 2 hours before the ICSI procedure. The specimen container must be clean, sterile and wide mouthed to minimize collection error. Oocyte retrieval: Under general anesthesia, the oocytes were aspirated by a specialized, ultrasound-guided needle (Labotect aspiration catheter, Germany) at 34-36 h after HCG injection. Warmed HEPES buffered medium (Irvine Scientific, Irvine, CA, USA) was used for handling and washing of oocytes. After ICSI, the whole injected oocytes were washed with Global total Fertilization Medium (Global pharm, Life Global, Brussels, Belgium, Europe) and the patients were randomly allocated into two equal groups (75 patients each) by using computer-based randomization program. Group one in which, the injected oocytes were transferred to a medium that contain 10 µmol of calcium ionophore (GM508 Cult-Active, Gynemed, Germany) and were incubated for 10 minutes, then again oocytes were washed with Global total Fertilization Medium (Global pharm, Life Global, Brussels, Belgium, Europe) and were incubated at 37°C in 6% CO2. In group two, the injected oocytes were not submitted to calcium ionophore activation. 18 hours after injection, the whole injected oocytes in both groups were evaluated for fertilization, cleavage and quality at the day of embryo transfer (ET). Embryo Transfer • After ET, luteal phase support was conducted (intramuscularly progesterone injection 100 mg daily) for 14 days until pregnancy test. After data collection, both groups were compared regarding oocyte number, oocyte fertilization rate, number and quality of embryos, implantation rate and clinical pregnancy rate.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility Primary

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
150 (Actual)

8. Arms, Groups, and Interventions

Arm Title
study group
Arm Type
Active Comparator
Arm Description
. This group involved 75 patients with history of fertilization failure in which oocytes were activated by calcium ionophores
Arm Title
control group
Arm Type
No Intervention
Arm Description
This group involved 75 patients with history of fertilization failure in which oocytes were not activated by calcium ionophores
Intervention Type
Drug
Intervention Name(s)
Calcium Ionophore A23187
Other Intervention Name(s)
non
Intervention Description
Calcium Ionophore A23187 is used in laboratories to increase intracellular Ca2+ levels in intact cells. It also uncouples oxidative phosphorylation, the process cells use to synthesize Adenosine triphosphate which they use for energy. In addition, A23187 inhibits mitochondrial ATPase activity. A23187 also induces apoptosis in some cells (e.g. mouse lymphoma cell line, or S49, and Jurkat cells) and prevents it in others (e.g. cells dependent on interleukin 3 that have had the factor withdrawn). In IVF field, Ca Ionophore can be used in case of low fertilization rate after ICSI procedure, particularly with Globozoospermia (Round Head sperm syndrome), Ca Ionophore will replace absence of sperm acrosom, and plays role in oocyte activation after ICSI. Recommended use is 0.5 microgram/ml twice for 10 min interrupted with fresh media with 30 min incubation, followed with regular injected eggs culture for IVF.
Primary Outcome Measure Information:
Title
fertilization rate
Description
the number of reproduced embryos divided by the number of fertilized oocytes
Time Frame
one and half year for all patients
Secondary Outcome Measure Information:
Title
Pregnancy rate
Description
the number of clinically pregnant women divided by the number of total patients undergoing ICSI procedures in the same group
Time Frame
one and half year for all patients

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: (1) Age between 20 and 40 years old. (2) Cases with history of total fertilization failure in previous ICSI cycles (3) Oocytes with normal morphology. Exclusion Criteria: (1) Abnormal oocyte morphology degenerated or immature oocytes. (2) Husbands with spermatogenic arrest or Sertoli/Leydig cells only.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
doaa DA aswad, Master
Organizational Affiliation
specialist of obstetrics and gynecology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Al-Azhar University
City
Cairo
State/Province
Nasr City
ZIP/Postal Code
17151
Country
Egypt

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

AOA in Recurrent Fertilization Failure

We'll reach out to this number within 24 hrs