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The Effect of RECO-18 on Infertile Women Undergoing in Vitro Fertilization-embryo Transfer

Primary Purpose

Fertility Disorders, Infertility, Female

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
RECO-18
Multi-vitamins
Sponsored by
Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Fertility Disorders focused on measuring pregnancy rate, in vitro fertilization-embryo transfer

Eligibility Criteria

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

Inclusion Criteria:

  • female, 20 to 40 years old
  • the 1st or 2nd cycle of IVF/ICSI treatment
  • BMI≤30Kg/m2
  • with bilateral ovaries
  • be eligible for IVF/ICSI treatment

Exclusion Criteria:

  • Repeated implantation failures (with previous 3 or more IVF/ICSI failures)
  • moderate to severe endometriosis
  • untreated hydrosalpinx
  • untreated endometrial disease
  • contraindications for assisted reproductive techniques or gestation
  • a history of ovarian surgery
  • expected poor ovarian response (POR) or previous POR
  • polycystic ovarian syndrome
  • participants in clinical trials of other drugs within one month prior to enrollment; • hypersensitivity to follicle-stimulating hormone α, FSH, human menopausal gonadotropin, LH or excipients
  • uncontrolled endocrine diseases (such as hyperthyroidism, hypothyroidism, adrenal gland disease, obesity, etc.)
  • percutaneous epididymal sperm aspiration or testicular sperm aspiration

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Experimental

    Arm Label

    Control group

    Treatment group

    Arm Description

    The control group takes the multi-vitamins (Elevit, Bayer S.A.) with the dosage of one tablet per day on the 1st to 5th day of menstruation, then perform ovulation induction on the second menstrual cycle, and continue to take multi-vitamins until the day of oocyte retrieval.

    The treatment group begins to take Reco-18 on the 1st to 5th day of menstruation with a dosage of 4 pills per day for the whole menstrual cycle, then perform ovulation induction on the second menstrual cycle, and continue to take Reco-18 until the day of oocyte retrieval.

    Outcomes

    Primary Outcome Measures

    Ongoing pregnancy rate at 12 weeks' gestation
    Gestational sac with embryocardia-beat detected on ultrasound at 12 weeks' gestation

    Secondary Outcome Measures

    Number of retrieved oocytes
    Total number of retrieved oocytes

    Full Information

    First Posted
    May 24, 2022
    Last Updated
    June 6, 2022
    Sponsor
    Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05412147
    Brief Title
    The Effect of RECO-18 on Infertile Women Undergoing in Vitro Fertilization-embryo Transfer
    Official Title
    A Pilot Study of the Effect of RECO-18 Containing Natural Plant Extracts on Infertile Women Undergoing in Vitro Fertilization-embryo Transfer
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    July 2022 (Anticipated)
    Primary Completion Date
    April 2023 (Anticipated)
    Study Completion Date
    April 2023 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University

    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

    5. Study Description

    Brief Summary
    How to improve the fertility of infertile women has become a hot topic in the field of assisted reproduction. Animal experiment has shown that RECO-18 significantly improved the female fertility in mice, and the specific mechanism was related to reducing follicular atresia, promoting follicle development and improving oocyte quality. Therefore the investigators aim to conduct a pilot study to explore the effect of RECO-18 in infertile women undergoing assisted reproduction treatment. This study is a prospective, randomized, controlled clinical study. The treatment group takes RECO-18 while the control group takes the multi-vitamins. The primary indicator is the ongoing pregnancy rate at 12 weeks' gestation; the secondary indicators are the number of oocytes retrieved, the normal fertilization rate and the rate of high quality embryos, implantation rate, clinical pregnancy rate, and early miscarriage rate.
    Detailed Description
    Mitochondrial function is closely related to oocyte quality in female. Deficiency of multiple micronutrients is common in infertile women, and supplementation with multiple micronutrients has antioxidant effects to reduce the damage of oxidative stress to fertility, and helps to improve the outcomes of assisted reproductive treatment. RECO-18 is a functional food containing a variety of plant extracts and enzymatic soy phospholipids. In in vivo and in vitro senescent models, the investigators found RECO-18 to improve oocyte quality mainly by regulating the mitochondrial apoptosis pathway. The investigators also found RECO-18 significantly improved the fertility of mice, and the specific mechanism was related to reducing follicular atresia, promoting follicle development and improving oocyte quality. Based on the animal experiments, the investigators intend to conduct a clinical trial to explore whether RECO-18 plays a role in improving oocyte and embryo quality and pregnancy outcomes in infertile women undergoing in vitro fertilization-embryo transfer.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Fertility Disorders, Infertility, Female
    Keywords
    pregnancy rate, in vitro fertilization-embryo transfer

    7. Study Design

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

    8. Arms, Groups, and Interventions

    Arm Title
    Control group
    Arm Type
    Active Comparator
    Arm Description
    The control group takes the multi-vitamins (Elevit, Bayer S.A.) with the dosage of one tablet per day on the 1st to 5th day of menstruation, then perform ovulation induction on the second menstrual cycle, and continue to take multi-vitamins until the day of oocyte retrieval.
    Arm Title
    Treatment group
    Arm Type
    Experimental
    Arm Description
    The treatment group begins to take Reco-18 on the 1st to 5th day of menstruation with a dosage of 4 pills per day for the whole menstrual cycle, then perform ovulation induction on the second menstrual cycle, and continue to take Reco-18 until the day of oocyte retrieval.
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    RECO-18
    Intervention Description
    4 pills daily, oral
    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    Multi-vitamins
    Intervention Description
    one tablet daily, oral
    Primary Outcome Measure Information:
    Title
    Ongoing pregnancy rate at 12 weeks' gestation
    Description
    Gestational sac with embryocardia-beat detected on ultrasound at 12 weeks' gestation
    Time Frame
    At 12 weeks' gestation
    Secondary Outcome Measure Information:
    Title
    Number of retrieved oocytes
    Description
    Total number of retrieved oocytes
    Time Frame
    Two weeks after oocyte retrieval
    Other Pre-specified Outcome Measures:
    Title
    The normal fertilization rate
    Description
    The rate of fertilization with two pronuclear
    Time Frame
    Two weeks after oocyte retrieval
    Title
    The rate of high quality embryos
    Description
    Number of high quality embryos / number of normal fertilized and cleavaged embryos
    Time Frame
    Two weeks after oocyte retrieval
    Title
    Implantation rate
    Description
    Number of gestational sac / number of transferred embryos
    Time Frame
    Four to five weeks after embryo transfer
    Title
    Clinical pregnancy rate
    Description
    Gestational sacs detected on ultrasound four to five weeks after embryo transfer
    Time Frame
    Four to five weeks after embryo transfer
    Title
    early miscarriage rate
    Description
    Misscarriage within 12 weeks' gestation
    Time Frame
    At 12 weeks' gestation

    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: female, 20 to 40 years old the 1st or 2nd cycle of IVF/ICSI treatment BMI≤30Kg/m2 with bilateral ovaries be eligible for IVF/ICSI treatment Exclusion Criteria: Repeated implantation failures (with previous 3 or more IVF/ICSI failures) moderate to severe endometriosis untreated hydrosalpinx untreated endometrial disease contraindications for assisted reproductive techniques or gestation a history of ovarian surgery expected poor ovarian response (POR) or previous POR polycystic ovarian syndrome participants in clinical trials of other drugs within one month prior to enrollment; • hypersensitivity to follicle-stimulating hormone α, FSH, human menopausal gonadotropin, LH or excipients uncontrolled endocrine diseases (such as hyperthyroidism, hypothyroidism, adrenal gland disease, obesity, etc.) percutaneous epididymal sperm aspiration or testicular sperm aspiration
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Yu Li, doctor
    Phone
    13660141860
    Email
    liyuliyu0922@163.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Dongzi Yang, doctor
    Organizational Affiliation
    Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
    Official's Role
    Study Director
    First Name & Middle Initial & Last Name & Degree
    Hui Chen, doctor
    Organizational Affiliation
    Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Ruiqi Li, doctor
    Organizational Affiliation
    Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Xiaoli Chen, doctor
    Organizational Affiliation
    Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Lin Li, doctor
    Organizational Affiliation
    Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Ping Pan, doctor
    Organizational Affiliation
    Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
    Official's Role
    Principal Investigator
    First Name & Middle Initial & Last Name & Degree
    Jia Huang, doctor
    Organizational Affiliation
    Sun Yat-Sen Memorial Hospital of Sun Yat-Sen University
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    The Effect of RECO-18 on Infertile Women Undergoing in Vitro Fertilization-embryo Transfer

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