RecruitingPhase 1Phase 2NCT06896747

Evaluating Mechanically Engineered Stem Cell Exosomes for Treating Endometrial Injury: A Clinical Study

Evaluation of the Therapeutic Effects of Mechanically Engineered Umbilical Cord-Derived Stem Cell Exosomes on Endometrial Injury: A Prospective, Non-Randomized, Parallel-Controlled Clinical Study


Sponsor

Tang-Du Hospital

Enrollment

90 participants

Start Date

Feb 21, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this clinical trial is to evaluate if engineered mechanically umbilical cord-derived stem cell exosomes, or conventional umbilical cord -derived stem cell exosomes, can improve endometrial thickness in women with thin endometrium. The main questions it aims to answer are: Can exosomes delivered via subendometrial injection improve endometrial thickness or clinical pregnancy rates compared to PRP (platelet-rich plasma)? Are there significant differences in endometrial thickness between the two treatment groups? Researchers will compare the intervention groups, which one group receives mechanical exosomes and the other receives conventional esosomes via subendometrial injection, to the control group, which receives PRP via the same methods, to see if exosomes provide superior therapeutic effects. Participants will: Receive either mechanical exosomesor or conventional esosomes or PRP through subendometrial injection. Be monitored for changes in endometrial parameters.


Eligibility

Sex: FEMALEMin Age: 20 YearsMax Age: 40 Years

Inclusion Criteria7

  • Females aged 20-40 years (inclusive of boundary values);
  • Normal ovarian reserve function (criteria: AFC ≥ 7, AMH > 1.1 ng/mL);
  • History of transcervical resection of adhesions (TCRA);
  • Received PRP treatment after TCRA;
  • At least one embryo transfer (ET) cycle in which they underwent standard ovarian stimulation (fresh cycle) or standard hormone replacement therapy (FET cycle), with an endometrial thickness of <7 mm;
  • Planned to continue IVF/ICSI/FET-assisted conception;
  • Able to accept and adhere to treatment and follow-up and willing to sign an informed consent form.

Exclusion Criteria12

  • Patients with severe systemic diseases, surgical contraindications, or cycle contraindications;
  • Patients with reproductive tract infections, genital tuberculosis, pelvic inflammatory disease, or malignant tumors of reproductive organs;
  • Patients with systemic diseases that cause uterine bleeding;
  • Patients allergic to any drugs, materials, or components used in this study;
  • Patients at high risk for hormone-dependent tumors such as breast cancer or ovarian tumors;
  • Patients with untreated submucosal fibroids of any size (FIGO 0/I/II), uterine fibroids ≥5 cm (FIGO III, IV, V, VI, VII), adenomyosis, unicornuate uterus, bicornuate uterus, or endometrial polyps;
  • Patients with hydrosalpinx ≥3 cm or hydrosalpinx of any size with significant vaginal discharge;
  • Patients with ovarian endometriotic cysts (chocolate cysts) ≥4 cm;
  • Patients who participated in other clinical trials within 3 months before surgery or during the study period;
  • Patients unable to tolerate anesthesia;
  • Patients with genetic abnormalities;
  • Other patients deemed unsuitable for participation in this study by the investigator.

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Interventions

BIOLOGICALMechanically Engineered Umbilical Cord Mesenchymal Stem Cell-Derived Exosomes

Mechanically engineered umbilical cord mesenchymal stem cell-derived exosomes (ME-UCMSC-Exo) are isolated from umbilical cord-derived mesenchymal stem cells (UCMSCs) subjected to mechanical stress conditioning during in vitro expansion. This process enhances exosome yield, bioactivity, and regenerative capacity. The exosomes are purified via ultracentrifugation and characterized for size, protein markers, and RNA content. In this study, ME-UCMSC-Exo is administered via intra-endometrial injection under hysteroscopic guidance. Each participant in this intervention group will receive 1-1.5 mL of exosome solution (containing approximately5\*10\^10 particles/mL) per injection site during the proliferative phase (Day 3-7 of the menstrual cycle). The aim is to enhance endometrial thickness, receptivity, and pregnancy outcomes in patients with thin endometrium secondary to intrauterine adhesions.

BIOLOGICALUmbilical cord mesenchymal stem cell-derived exosomes

Umbilical cord mesenchymal stem cell-derived exosomes (UCMSC-Exo) are obtained from standard cultured UCMSCs without mechanical stress preconditioning. These exosomes undergo identical purification and characterization procedures as ME-UCMSC-Exo but lack biomechanical priming. UCMSC-Exo is also administered intra-endometrially via hysteroscopic injection at a dose of 1-1.5 mL (5\*10\^10 particles/mL) per site.

BIOLOGICALplatelet-rich plasma

Platelet-rich plasma (PRP) is an autologous biological preparation obtained from centrifuged whole blood. It contains a high concentration of growth factors, including platelet-derived growth factor (PDGF), transforming growth factor-beta (TGF-β), and vascular endothelial growth factor (VEGF), which promote endometrial regeneration. In this study, PRP will be administered via hysteroscopically guided intra-endometrial injection at a dose of 1-1.5 mL per injection site, following standard PRP preparation protocols. This group serves as a positive control for evaluating the efficacy of exosome-based therapies.


Locations(2)

Tang-Du Hospital

Xi'an, Shaanxi, China

Tang-Du Hospital

Xi'an, Shaanxi, China

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