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Improvement of Live Babies Rates After ICSI, Using cpFT (FERTICSI)

Primary Purpose

Infertility, Oocyte, Pregnancy

Status
Recruiting
Phase
Phase 3
Locations
France
Study Type
Interventional
Intervention
Cyclic peptide Fertiline
Sponsored by
Assistance Publique - Hôpitaux de Paris
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Infertility focused on measuring Infertility, Femal infertility, Assisted Reproduction Technology outcome

Eligibility Criteria

18 Years - 36 Years (Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Couples eligible for a first attempt at Assisted Reproduction (AMP).
  • Couples asking for Assisted Reproductive Technology, and requiring an ICS procedure.
  • Women aged 18 to 36 inclusive.
  • Men aged 18 to 58 inclusive
  • Use of CSCM-C culture medium from Biocare / Irvine, exclusively.
  • People affiliated to a Social Security scheme

Exclusion Criteria:

  • Lack of consent
  • Early menopause.
  • Couples under IVF or Intra Uterine Insemination treatment.
  • Patients resumed after a first attempt by the couple.
  • People unable to follow protocol visits in France.
  • Couple with a contraindication to treatment with ART.
  • Women with a contraindication to treatment with ART or an associated pathology such as: hypertension, risk of eclampsia, viral risk, family genetic problems, diabetes, uterine partitions, synechiae adhesions, adenomyosis or any other contraindication judged as such by the investigator.
  • AMP with donation of gametes or embryos.
  • Frozen sperm.
  • Participant under guardianship or guardianship

Sites / Locations

  • Department Biology of Reproduction, Hospital Cochin AP-HPRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

Fertiline group

Control group

Arm Description

Treated by supplementation of the culture medium with the molecule.

No supplementation

Outcomes

Primary Outcome Measures

Live birth rate after the first embryo transfer
Demonstration of the improvement in the rate of live births after ICSI by supplementing the pre-ICSI incubation medium of oocytes and that of preimplantation embryos with cpFT (1µM) during the 1st embryo transfer in women under 37 years of age.

Secondary Outcome Measures

Level of Metaphase II oocytes
Quality of the embryonic culture
The measure evaluates the rate and number of fertilized eggs over the total number of metaphase 2 oocytes.
Evaluation of the kinetics of embryonic development when possible.
The embryos will be kept in an incubator with an embryoscope so that their cleavage sequences will be registered "when possible". The criteria will analysis the cleavage sequences of all embryos during preimplantation embryogenesis.
Embryonic quality at the blastocyst stage
All the embryos that will reach the blastocyst stage will be evaluated according to the Gardner criteria.
Quality of the embryos after vitrification
The percentage of Good and Top embryos after thawing will be compared to the grading for the same embryo before cryopreservation according to Gardner criteria
Implantation rate with positive Beta hCG after transfer
Clinical pregnancy rates with cardiac activity
The rate of miscarriages per pregnancy
rate of abnormality on morphological ultrasounds
It reports the percentage of morphological ultrasounds showing an abnormality in the fetus morphology on the total number of morphological ultrasounds performed for all the pregnancies depending of the study.
rate of neonatal abnormality
It reports the percentage of neonatal baby examination showing an abnormality over the total number of neonatal baby examination performed for all the babies who will born during the study.
children's development
It reports the percentage of one year old baby examinations showing an abnormality over the total number of one year old baby examinations performed for all the babies who will born during the study.

Full Information

First Posted
April 29, 2021
Last Updated
November 14, 2022
Sponsor
Assistance Publique - Hôpitaux de Paris
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1. Study Identification

Unique Protocol Identification Number
NCT04954274
Brief Title
Improvement of Live Babies Rates After ICSI, Using cpFT
Acronym
FERTICSI
Official Title
Improvement of Live Babies Rates After ICSI, Using cpFT: Multicenter Prospective Randomized Clinical Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Recruiting
Study Start Date
July 29, 2021 (Actual)
Primary Completion Date
August 26, 2023 (Anticipated)
Study Completion Date
August 26, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris

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
Demonstrate the improvement of the live births rate after ICSI by supplementing the pre-ICSI incubation medium of oocytes and that of preimplantation embryos with cpFT at the 1st embryo transfer for women under 37 years old.
Detailed Description
Supplementation of the incubation medium with cFEE should improve the implantation rate and ART outcome. As in France ICSI is widely used to achieve good fertilization rates, we decided to use ICSI to fertilize the egg, and the peptide: to improve chromosome segregation during meiosis, and to improve in vitro embryogenesis after ICSI. Hence the protocol includes an oocyte preincubation step prior to ICSI and a co incubation of the embryo with the molecule during blastocyst formation. Hence our protocol includes: - a preincubation of the decoronized oocytes with the peptide prior to ICSI, and - a coincubation of the developing embryo with the molecule. The principal criteria will be the live baby rate after the first embryo transfer (using the best embryo). As the oocyte loses its strength as the women is getting older, the main criteria will be evaluated for women under 37 years old. Randomization: every couple will be randomly assigned to the Control or the Treated group. Treated group: After egg retrieval, the oocyte will be decoronized and incubated prior to ICSI procedure into CSCM-C (Irvine) medium supplemented with the molecule. Control group: similar protocol of incubation but without the molecule. After ICSI the zygote will be incubated until the blastocyste stage in CSCM-C medium (Irvine). Embryo transfer will be limited to only one blastocyst, fresh or delayed after cryopreservation.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Oocyte, Pregnancy
Keywords
Infertility, Femal infertility, Assisted Reproduction Technology outcome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
there will be two groups: one treated by supplementation of the culture medium with 1 Micromolar of the molecule, the other being the control group.
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
366 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Fertiline group
Arm Type
Experimental
Arm Description
Treated by supplementation of the culture medium with the molecule.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
No supplementation
Intervention Type
Drug
Intervention Name(s)
Cyclic peptide Fertiline
Other Intervention Name(s)
cFEE
Intervention Description
Upon retrieval, the oocyte will be decoronized and incubated prior to ICSI procedure into CSCC-M medium supplemented with the molecule. After ICSI, the zygote will be incubated in CSCM-C medium supplemented with the peptide.
Primary Outcome Measure Information:
Title
Live birth rate after the first embryo transfer
Description
Demonstration of the improvement in the rate of live births after ICSI by supplementing the pre-ICSI incubation medium of oocytes and that of preimplantation embryos with cpFT (1µM) during the 1st embryo transfer in women under 37 years of age.
Time Frame
28 months after the first inclusion
Secondary Outcome Measure Information:
Title
Level of Metaphase II oocytes
Time Frame
Through study completion average 16 months
Title
Quality of the embryonic culture
Description
The measure evaluates the rate and number of fertilized eggs over the total number of metaphase 2 oocytes.
Time Frame
16 months after the first inclusion
Title
Evaluation of the kinetics of embryonic development when possible.
Description
The embryos will be kept in an incubator with an embryoscope so that their cleavage sequences will be registered "when possible". The criteria will analysis the cleavage sequences of all embryos during preimplantation embryogenesis.
Time Frame
16 months after the first inclusion
Title
Embryonic quality at the blastocyst stage
Description
All the embryos that will reach the blastocyst stage will be evaluated according to the Gardner criteria.
Time Frame
Day 5-6 after ICSI
Title
Quality of the embryos after vitrification
Description
The percentage of Good and Top embryos after thawing will be compared to the grading for the same embryo before cryopreservation according to Gardner criteria
Time Frame
Day 5-6 after ICSI
Title
Implantation rate with positive Beta hCG after transfer
Time Frame
20 months after the first inclusion
Title
Clinical pregnancy rates with cardiac activity
Time Frame
22 months after the first inclusion
Title
The rate of miscarriages per pregnancy
Time Frame
22 months after the first inclusion
Title
rate of abnormality on morphological ultrasounds
Description
It reports the percentage of morphological ultrasounds showing an abnormality in the fetus morphology on the total number of morphological ultrasounds performed for all the pregnancies depending of the study.
Time Frame
28 months after the beginning of the study
Title
rate of neonatal abnormality
Description
It reports the percentage of neonatal baby examination showing an abnormality over the total number of neonatal baby examination performed for all the babies who will born during the study.
Time Frame
28 months after the beginning of the study
Title
children's development
Description
It reports the percentage of one year old baby examinations showing an abnormality over the total number of one year old baby examinations performed for all the babies who will born during the study.
Time Frame
45 months after the beginning of the study

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
36 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Couples eligible for a first attempt at Assisted Reproduction (AMP). Couples asking for Assisted Reproductive Technology, and requiring an ICS procedure. Women aged 18 to 36 inclusive. Men aged 18 to 58 inclusive Use of CSCM-C culture medium from Biocare / Irvine, exclusively. People affiliated to a Social Security scheme Exclusion Criteria: Lack of consent Early menopause. Couples under IVF or Intra Uterine Insemination treatment. Patients resumed after a first attempt by the couple. People unable to follow protocol visits in France. Couple with a contraindication to treatment with ART. Women with a contraindication to treatment with ART or an associated pathology such as: hypertension, risk of eclampsia, viral risk, family genetic problems, diabetes, uterine partitions, synechiae adhesions, adenomyosis or any other contraindication judged as such by the investigator. AMP with donation of gametes or embryos. Frozen sperm. Participant under guardianship or guardianship
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jean Philippe Mr WOLF, MD-PhD
Phone
01 58 41 37 31
Ext
+33
Email
jean-philippe.wolf@aphp.fr
First Name & Middle Initial & Last Name or Official Title & Degree
Catherine PATRAT, MD-PhD
Phone
01 58 41 37 34
Ext
+33
Email
catherine.patrat@aphp.fr
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean Philippe Mr WOLF, MD-PhD
Organizational Affiliation
AP-HP, Hospital Cochin
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department Biology of Reproduction, Hospital Cochin AP-HP
City
Paris
ZIP/Postal Code
75014
Country
France
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jean Philippe Mr WOLF, MD-PhD
Phone
33 1 58 41 37 31
Ext
0033
Email
jean-philippe.wolf@aphp.fr

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
18692807
Citation
Barraud-Lange V, Naud-Barriant N, Ducot B, Chambris S, Bomsel M, Wolf JP, Ziyyat A. Cyclic QDE peptide increases fertilization rates and provides healthy pups in mouse. Fertil Steril. 2009 May;91(5 Suppl):2110-5. doi: 10.1016/j.fertnstert.2008.05.088. Epub 2008 Aug 9.
Results Reference
background
PubMed Identifier
16096325
Citation
Ziyyat A, Naud-Barriant N, Barraud-Lange V, Chevalier F, Kulski O, Lemkecher T, Bomsel M, Wolf JP. Cyclic FEE peptide increases human gamete fusion and potentiates its RGD-induced inhibition. Hum Reprod. 2005 Dec;20(12):3452-8. doi: 10.1093/humrep/dei241. Epub 2005 Aug 11.
Results Reference
background

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Improvement of Live Babies Rates After ICSI, Using cpFT

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