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Completed

NCT Number: NCT05703308

Menstrual Blood Stem Cells in Poor Ovarian Responders

In this controlled trial, poor ovarian responder women will be treated with transplantation of autologous menstrual blood stem cells. The investigators will attempt to assess the safety and efficacy of this procedure for the treatment of infertility in POR patients compared to control group.

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Key information

Age range

25 year–45 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 3

Primary location

Avicenna Research Institute

Tehran, Iran

About this study

With economic development, procreation delays have resulted in more women seeking medical help for infertility treatment. Because the quality and quantity of oocytes are affected by physiological age, despite advances in assisted reproductive technology (ART), managing infertility in women with poor ovarian response (POR) remains a daily challenge for physicians.

Adult mesenchymal stromal cell (MSC) therapy has gained particular interest in recent years because it may provide a supportive microenvironment for oocyte development from quiescent primordial follicles. Human MSC transplantation has been shown in preclinical studies to host ovaries and restore their function and structure premature ovarian failure (POF) animal models.

Because of their encouraging characteristics such as ease of access, high availability, monthly repeatability of sampling, less ethical considerations, lack of tumor-causing potential, protected property, and significant trans-differentiation capacity, endometrial-derived stromal cells have been considered in a wide range of studies since 2007. Menstrual blood-derived stromal cells (MenSCs), on the other hand, are derived from endometrial tissue and can be collected in a non-invasive manner, making them especially useful in the treatment of reproductive disorders. The investigators attempted to assess the safety and efficacy of intraovarian injection of MenSCs for the treatment of infertility in POR patients based on this evidence.

The results of this clinical trial's phases I and II indicated that Men-MSCs could be considered as a potential treatment to restore the fertility capability of POR women. Based on these findings, the investigators have designed a Phase III controlled trial of autologous MenSC therapy for patients with POR.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Serum AMH < 0.1 ng/ml (at the screening visit and in the absence of OC or sex-steroid intake)
  • Antral follicular count (AFC) in both ovaries < 4 (at screening visit and in the absence of OC or sex-steroid intake)
  • Positive history of at least1 standard previous IVF-ET or ICSI-ET
  • Normal thyroid hormones (TSH and FT4)
  • Normal level of prolactin,
  • Normal level of fasting blood sugar
  • Normal Liver tests (SGOT, SGPT)
  • Normal level of BUN, creatinine
  • Negative Infectious tests (HIV, HCV, HBS Ag, VDRL)
  • Normal coagulation factors (PT, PTT, BT, CT)
  • Normal serum levels of sodium, potassium, calcium, phosphorus
  • Negative history of endometrioma or other ovarian cysts
  • Negative history of previous ovarian surgery
  • Negative history of cancer
  • Negative history of a known autoimmune disorder.

Exclusion criteria

  • Positive history of hydrosalpinx or anatomical uterine disorders (In vaginal sonography or HSG)
  • Severe male factors of their husbands (count <15 million/ml)

Treatment and study plan

Autologous Menstrual Blood Stem Cells

Biological

The menstrual blood of patients in the MenSCs treatment group was collected in sterile menstrual cups on the second day of menstruation, and directly transferred to a class B clean room for MSC isolation and culture. All cell quality control studies were performed prior to the International Conference of Harmonization Q2 (ICH Q2) guidelines. The density of the final product was 20×106 cells/ml. 150 μl of the prepared suspension was injected intravaginally into each ovary of the patient under general anaesthesia

Primary outcomes

  1. Spontaneous pregnancy rate

    Time frame: 3 months after stem cell injection

    Number of participants that establish a spontaneous clinical pregnancy after stem cell injection

  2. Pregnancy rate after ICSI

    Time frame: 4 weeks after embryo transfer

    Number of participants that establish a clinical pregnancy after embryo transfer

Secondary outcomes

  1. Hormone levels

    Time frame: 2 and 4 months after stem cell injection

    Change from baseline in Anti-Müllerian hormone (AMH), serum follicle stimulating hormone (FSH), and antral follicle count (AFC)

  2. Number of oocytes

    Time frame: Day 0 after follicle puncture

    Mean number of retrieved COCs per protocol

  3. Number of MII oocytes

    Time frame: Day 0 after follicle puncture

    Mean number of metaphase II (MII) oocytes per protocol

  4. Number of embryos

    Time frame: Day 3-5 after follicle puncture

    Mean number of embryos

  5. Number of high quality embryos number

    Time frame: Day 3-5 after follicle puncture

    Grade A for cleavage stage embryo, >=3BB for blastocyst

  6. Clinical pregnancy rate

    Time frame: 4 weeks after embryo transfer

    The incidence of gestational sac with heartbeat assessed by TVS

  7. Biochemical pregnancy rate

    Time frame: 12-16 days after oocyte pick-up

    Incidence of serum beta-hCG test > 25 mIU/ml

  8. Live birth rate

    Time frame: at a follow-up time of 30 days after delivery

    Incidence of the birth of at least one live newborn after 22 weeks of gestation

  9. Incidence of Treatment-Emergent Adverse Events [Safety and Tolerability]

    Time frame: at a follow-up time after 1 year

    Incidence of adverse and serious adverse events with potential relationship to treatment

Sponsors and collaborators

Lead sponsor

Avicenna Research Institute

Other

Registry information

Official study title

Outcome of Pregnancy in Poor Ovarian Responders by Intraovarian Administration of Autologous Menstrual Blood Derived-Mesenchymal Stromal Cells

Important dates

Study start
2020
Primary completion
2021
Study completion
2022
First posted
Jan 30, 2023
Registry last updated
Jan 30, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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