Myo-inositol for the Management of Poor Ovarian Responders: A Prospective Randomized Controlled Trial

Sponsor
American University of Beirut Medical Center (Other)
Overall Status
Recruiting
CT.gov ID
NCT04273256
Collaborator
(none)
226
1
2
35.7
6.3

Study Details

Study Description

Brief Summary

The management of poor ovarian responders (POR) remains the most challenging in In-Vitro Fertilization (IVF). The incidence of POR ranges between 9 and 24% (Caprio F, et al, 2015).

POR refers to a reduction in the quantity of primordial follicle pool in reproductive age group (Jirge, P. R., 2016, Sunkara, S. K., et al, 2014), in addition to a higher risk of implantation failure (Kailasam C, et al, 2004).

To overcome this condition, fertility treatments using controlled ovarian stimulation along with IVF is needed to achieve pregnancy. Despite the use of various treatments including high dose gonadotropins, patients with POR have lower rates of pregnancy compared to patients with normal ovarian response (Oudendijk, J. F., et al, 2011). Studies now suggest a variety of regimens like the use of growth hormones, DHEA or androgens to improve the outcomes (Kyrou D, et al, 2009). The main interest of this study is the use of myo-inositol prior to IVF cycles for improvement of reproductive outcomes in poor ovarian responders.

Condition or Disease Intervention/Treatment Phase
Phase 2/Phase 3

Detailed Description

The management of poor ovarian responders (POR) remains the most challenging in In-Vitro Fertilization (IVF). The incidence of POR ranges between 9 and 24% (Caprio F, et al, 2015).

POR refers to a reduction in the quantity of primordial follicle pool in reproductive age group (Jirge, P. R., 2016, Sunkara, S. K., et al, 2014), in addition to a higher risk of implantation failure (Kailasam C, et al, 2004).

To overcome this condition, adjuvant fertility treatments using controlled ovarian stimulation along with IVF is needed to achieve pregnancy. Despite the use of various treatments including high dose gonadotropins, patients with POR have lower rates of pregnancy compared to patients with normal ovarian response (Oudendijk, J. F., et al, 2011). Studies now suggest a variety of regimens like the use of growth hormones, DHEA or androgens to improve the outcomes (Kyrou D, et al, 2009).

Inositol belongs to the vitamin B group, precursor for the synthesis of phosphatidylinositol polyphosphates (PIPs). PIPs belong to the signal transduction system involved in the regulation of different cellular functions such as signal transduction, cell morphogenesis and cytogenesis (Kutateladze TG, 2010). It is involved in cell membrane formation, lipid synthesis and cell growth (Unfer V, et al, 2012). It has been extensively studied in patients with insulin resistance, as inositol has an insulin sensitizing action (Croze ML & Soulage CO, 2013). In addition, researchers have hypothesized different mechanisms of action on different cell types especially at the level of the ovaries. An international consensus has confirmed that myo-inositol pre-treatment is able to improve the oocyte and the embryo quality via enhancing the intracellular Ca2+ oscillation with meiotic progression of germinal vesicle oocytes. Therefore, it acts on improving the oocyte maturation and embryo development (Nestler JE, et al, 1999, Papaleo E, et al, 2009).

Previous studies showed that higher concentrations of myo-inositol in follicular fluid are correlated with a better oocyte quality (Chiu TT, et al, 2002). A study by Jiang demonstrated that inositol supplementation reduces oxidative stress by different agents such as increasing superoxide dismutase and catalase levels (Jiang WD, et al, 2011). In view of its effects on oocyte maturation and quality, the use of myo-inositol in women with POR is promising. However, data is still sparse whether supplementation with myo-inostiol prior to IVF cycles does improve the pregnancy outcomes.

The main interest of this study is the use of myo-inositol prior to IVF cycles for improvement of reproductive outcomes in poor ovarian responders.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
226 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Upon consent, recruited women will be randomly allocated into either one of the study groups using a simple randomization method by computer-generated random numbersUpon consent, recruited women will be randomly allocated into either one of the study groups using a simple randomization method by computer-generated random numbers
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Myo-inositol for the Management of Poor Ovarian Responders: A Prospective Randomized Controlled Trial
Actual Study Start Date :
Feb 11, 2020
Anticipated Primary Completion Date :
Feb 1, 2022
Anticipated Study Completion Date :
Feb 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Myo-inositol arm

Patients will be supplemented with 2 grams of Myo-inositol + at least 400 μg of folic acid (received from routinely prescribed multivitamins) every day for 3 months before the IVF cycle.

Drug: Myo-inositol
patients who will be supplemented with 2 grams of Myo-inositol daily for 3 months prior to their in-vitro fertilization cycle
Other Names:
  • Celine
  • No Intervention: Control arm

    Patients will receive at least 400 μg of folic acid from routinely prescribed multivitamins every day for 3 months before the IVF cycle.

    Outcome Measures

    Primary Outcome Measures

    1. Retrieved oocytes [4 months]

      Number of oocytes retrieved (MII), including total number, number of mature MII, and proportion of dysmorphic oocytes

    Secondary Outcome Measures

    1. Cycle cancellation rate [4 months]

      number of cycles cancelled before reaching embryo transfer

    2. Fertilization rate [4 months]

      number of zygotes per number of oocytes inseminated

    3. Implantation rate [5 months]

      number of intrauterine gestational sacs observed on transvaginal ultrasound divided by the number of transferred embryos

    4. Clinical pregnancy rate per started treatment cycle (CPR) [6 months]

      the presence of a fetal heart beat on transvaginal ultrasound after 6-7 weeks of gestation

    5. Ongoing pregnancy per embryo transferred [7 months]

      number of viable fetuses beyond 20 weeks' gestation per number of embryos transferred

    6. Miscarriage rates [7 months]

      pregnancy loss prior to 12 weeks' gestation

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 44 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Age: 18-44 years at the time of interview

    • POR patients defined as: AMH<1.5 ng/nl, AFC of 7 or less, 5 oocytes or less retrieved in a previous cycle

    • Patients undergoing controlled ovarian stimulation for any indication:

    • Male factor

    • Female factor

    Exclusion Criteria:
    • Patients with diabetes, thyroid dysfunction

    • Patients with abnormal uterine cavity

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 American University of Beirut Medical Center Beirut Lebanon

    Sponsors and Collaborators

    • American University of Beirut Medical Center

    Investigators

    • Principal Investigator: Antoine Abu Mussa, MD, American University of Beirut Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Antoine Abou Moussa, professor of Obstetrics and Gynecology, American University of Beirut Medical Center
    ClinicalTrials.gov Identifier:
    NCT04273256
    Other Study ID Numbers:
    • BIO-2018-0357
    First Posted:
    Feb 18, 2020
    Last Update Posted:
    Feb 18, 2020
    Last Verified:
    Feb 1, 2020
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Antoine Abou Moussa, professor of Obstetrics and Gynecology, American University of Beirut Medical Center
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 18, 2020