search
Back to results

Improvement of IVF Fertilization Rates, by the Cyclic Tripeptide FEE - Prospective Randomized Study (Fertiline)

Primary Purpose

Infertility, Pregnancy

Status
Terminated
Phase
Not Applicable
Locations
France
Study Type
Interventional
Intervention
cFFE increase the fusiogenic capacities of a gamete
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 tripeptide FEE, fertilization rates, embryos, oocytes

Eligibility Criteria

18 Years - 43 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients eligible for in vitro fertilization except indication of ICSI. That is to say : the patients whose sperm has the following characteristics :

    • Sperm count over 107 spz /ml and Mobility * ( a + b ) is greater than 15 %
    • Typical forms above 10%
  • Women aged 18 to 43 years.
  • Patients gave their informed written consent
  • People affiliated to a social security system

Exclusion Criteria:

  • Patients whose sperm indicates the use or ICSI
  • Patients who have not given their consent or without the consent of one of the two spouses
  • Ovarian failure , menopause

Sites / Locations

  • Wolf

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

group cFEE

untreated group

Arm Description

The group cFEE will be similarly inseminated with 100000/ml motile spermatozoa and will be supplemented with cFEE 100µM during 18 hours. The cFEE will increase the fusiogenic capacities of a gamete,

control group

Outcomes

Primary Outcome Measures

Fertilization rates

Secondary Outcome Measures

Embryo quality
The embryo quality will be assessed according to the number of blastomeres, the presence of cytoplasmic fragments, multinucleated blastomeres, they shape and regularity, and their cleavage rate. Data will be compared to the Z score classification for the zygote, and the Gardner classification for the blastocyste.
Pregnancy outcome
Baby health
Baby health will be assessed on data collected during the pregnancy by the OBGYN, the 6 month ultrasound examination, and the health of the baby at delivery. It will consider the APGAR index and its weight and stature. During the first year of life, the baby health will be assessed by the pediatrician's examination at 6 month and one year old.

Full Information

First Posted
April 28, 2014
Last Updated
May 25, 2020
Sponsor
Assistance Publique - Hôpitaux de Paris
search

1. Study Identification

Unique Protocol Identification Number
NCT02161861
Brief Title
Improvement of IVF Fertilization Rates, by the Cyclic Tripeptide FEE - Prospective Randomized Study
Acronym
Fertiline
Official Title
Improvement of IVF Fertilization Rates, by the Cyclic Tripeptide FEE - Prospective Randomized Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Terminated
Why Stopped
the trial was discontinued for legislative reasons.
Study Start Date
September 8, 2014 (Actual)
Primary Completion Date
October 2015 (Actual)
Study Completion Date
April 2016 (Actual)

3. Sponsor/Collaborators

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

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
cFEE peptide improves the IVF fertilization rate in mouse and fertilization index in human. It improves sperm movement's parameters. It has been studied over 3 generations of mice and appears without any side effects. The Agence de la BioMédecine has given the authorization for testing the peptide in human IVF. It is expected to improve the fertilization rate, and thus provide more embryos per IVF attempt. 160 couples will be included over 15 months. Patient sperm parameters should be suitable for IVF. Female should be between 18 and 43 year old. Each cohort of eggs will be randomly distributed to one of the 2 groups The first group will be inseminated with 100000/ml motile spermatozoa. The second will be similarly inseminated but in a middle which will be supplemented with cFEE 100µM. Criteria: number of embryos in each group
Detailed Description
Name and address of the coordinating investigator : Prof. Jean Philippe Wolf, Histology - Embryology Department , Biology of Reproduction - . Cochin Hospital , 123 Bd Port Royal, 75014 Paris Promotor: AP- HP represented by DRCD - Hôpital Saint- Louis Inclusion Sites : CHU Cochin, Paris Main objective: - To improve fertilization rate in IVF by supplementation of culture media with a molecule increasing the sperm fertilizing ability. Secondary objectives Compare the rates of cleavage between the two groups of zygotes Compare the percentage of good quality embryos Number of patients : 160 Duration of the inclusion period : 15 months Duration of participation of the patient: For each couple, the duration of participation will be as many times nine months that pregnancies will be obtained from fresh or frozen embryo transfers.In the absence of pregnancy duration of participation will be only 15 days. Time monitoring of children : 9 months Total study duration : The total study duration will be 36 months Rational : The cyclic tripeptide FEEc reproduces the binding site of Fertilin Beta. It binds to the alpha 6 beta 1 integrin and increases sperm fertilizing ability, improving its movement's parameters . Added to insemination IVF media, it should increase fertilization rates . Methodology: Oocytes in each cohort will be divided into two groups, one of which will be inseminated with the control medium and the other group is inseminated in the presence of peptide. The fertilization rate and embryo quality will be compared between these two groups. Statistical analysis: In mice with healthy gamete, the observed fertilization rate increase in the presence of peptide was 100 %. The fertilization rate in human IVF is about 65%, male indications included. There is an improvement of the fertilization index of zona free human oocytes of about 90% . We can reasonably foresee an improvement of 15 % of the fertilization rate in normal IVF. This is why we believe that the difference between fertilization rates of both treated and control groups must be meaningful for 160 attempts. In this calculation it was assumed that the intra cluster correlation (ie intra cohort oocyte ) resulted in a 'design effect' D equal to 4. The analysis will include descriptive statistics for each quantitative parameter at each time : mean, standard deviation , minimum, maximum , median and quartiles , number of missing values . Quality parameters will be expressed by their frequency of distribution and associated 95% bilateral confidence intervals.The distributions of the numbers of blastomeres per embryo will be compared between the two groups by exact permutation test (stratified). This method is more suitable than "naive" comparison of these numbers, since it takes into account the possible correlation between results for embryos belonging to the same embryo cohort (Gibbons JD 1985 Non parametric statistical inference - Marcel Dekker New York ). The cellular index, the pregnancy rate, spontaneous abortions, therapeutic abortion, childbirth, will be compared using Student's t test and exact Fisher test. All tests will be bilateral, and look for possible negative effects, set at 5%. Calculations will be performed using SAS statistical software v9.13 (SAS Institute, Cary , NC) under the supervision of Professor Eric Vicaut URC Lariboisière St. Louis. Primary endpoint : Rate of fertilization Expected Benefits : Improved fertilization rates of at least 15 %

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Infertility, Pregnancy
Keywords
tripeptide FEE, fertilization rates, embryos, oocytes

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
66 (Actual)

8. Arms, Groups, and Interventions

Arm Title
group cFEE
Arm Type
Experimental
Arm Description
The group cFEE will be similarly inseminated with 100000/ml motile spermatozoa and will be supplemented with cFEE 100µM during 18 hours. The cFEE will increase the fusiogenic capacities of a gamete,
Arm Title
untreated group
Arm Type
No Intervention
Arm Description
control group
Intervention Type
Other
Intervention Name(s)
cFFE increase the fusiogenic capacities of a gamete
Other Intervention Name(s)
The cyclic tripeptide
Primary Outcome Measure Information:
Title
Fertilization rates
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
Embryo quality
Description
The embryo quality will be assessed according to the number of blastomeres, the presence of cytoplasmic fragments, multinucleated blastomeres, they shape and regularity, and their cleavage rate. Data will be compared to the Z score classification for the zygote, and the Gardner classification for the blastocyste.
Time Frame
day 5
Title
Pregnancy outcome
Time Frame
9 months
Title
Baby health
Description
Baby health will be assessed on data collected during the pregnancy by the OBGYN, the 6 month ultrasound examination, and the health of the baby at delivery. It will consider the APGAR index and its weight and stature. During the first year of life, the baby health will be assessed by the pediatrician's examination at 6 month and one year old.
Time Frame
Year one

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
43 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients eligible for in vitro fertilization except indication of ICSI. That is to say : the patients whose sperm has the following characteristics : Sperm count over 107 spz /ml and Mobility * ( a + b ) is greater than 15 % Typical forms above 10% Women aged 18 to 43 years. Patients gave their informed written consent People affiliated to a social security system Exclusion Criteria: Patients whose sperm indicates the use or ICSI Patients who have not given their consent or without the consent of one of the two spouses Ovarian failure , menopause
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jean-philippe Wolf, MD
Organizational Affiliation
Embryology Department , Biology of Reproduction - . Cochin Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Wolf
City
Paris
ZIP/Postal Code
75014
Country
France

12. IPD Sharing Statement

Citations:
PubMed Identifier
9105040
Citation
Yuan R, Primakoff P, Myles DG. A role for the disintegrin domain of cyritestin, a sperm surface protein belonging to the ADAM family, in mouse sperm-egg plasma membrane adhesion and fusion. J Cell Biol. 1997 Apr 7;137(1):105-12. doi: 10.1083/jcb.137.1.105.
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
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
Citation
Wolf JP, Bomsel M. Brevet international "Peptide augmentant la capacité fusiogène d'une gamète" Université Paris 13 et CNRS. N° d'enregistrement 03 13545 ; N° de publication 2 862 225. 2003
Results Reference
background

Learn more about this trial

Improvement of IVF Fertilization Rates, by the Cyclic Tripeptide FEE - Prospective Randomized Study

We'll reach out to this number within 24 hrs