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The effect of human umbilical cord matrix stem cell transplantation therapy on pregnancy rate of patient with premature ovarian failure and endometrial repair disorders

The effect of human umbilical cord matrix stem cell transplantation therapy on pregnancy rate of patient with premature ovarian failure and endometrial repair disorders

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021618
Enrollment
Unknown
Registered
2019-03-01
Start date
2019-05-01
Completion date
Unknown
Last updated
2019-03-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

premature ovarian failure and endometrial repair disorders

Interventions

1:Conventional hormone replacement therapy combined with hysteroscopic curettage
2:Conventional hormone replacement therapy combined with hysteroscopic curettage + huc-mscs ovarian transplantation
3:Conventional hormone replacement therapy combined with hysteroscopic curettage + huc-mscs intrauterine transplantation
4:Conventional hormone replacement therapy combined with hysteroscopic curettage + huc-mscs ovary and uterine transplantation

Sponsors

First Maternity and Infant Hospital Affiliated to Tongji University
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1. female aged 20-40 years with fertility requirement, diagnosed as premature ovarian failure (premature ovarian failure group) and severe intrauterine adhesion and thin uterus (endometrium repair); 2. for premature ovarian failure group: serum FSH > 40 IU/L was detected twice everay 4-6 weeks, and amenorrhea occurred for 4 month. For endometriial repair group: who were diagnosed with severe intrauterine adhesion of who still had intrauterine adhesion after two or more intrauterine surgeries, and thickness less than 7 mm; 3. sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. abnormal karyotype or RIF family history; 2. autoimmune disease, or ovarian or adrenal autoantibody screening positive; 3. polycystic ovary syndrome; 4. high GnRH sensitivity; 5. severe endometriosis; 6. breast cancer and ovarian cancer; 7. other malignant tumors, hepatitis and other diseases; 8. HIV +; 9. BMI >30; 10. have a history of surgery or other related diseases.

Design outcomes

Primary

MeasureTime frame
Clinical pregnancy rate;No complication delivery rate;

Secondary

MeasureTime frame
endometrial thickness;morphology of the uterine cavity;Uterine arterial blood flow;Uterine receptivity markers;Pulse index and resistance index of uterine artery;Serum hormone concentration: FSH, LH, E2, P4 and AMH;Menstrual status;ovarian volume;Number of follicles;Dominant follicle count;Ovarian blood flow;The responsiveness of ovaries to gonadotropins;The number of oocytes that are available;In vitro fertilization rate and high quality embryo rate;Success rate of planting;No complication delivery rate;The proportion of immune cells in the blood: CD3-/CD56+ NK cell, Th1/Th2, CD3+IL-17+ T cell, CD4+IL-17+ T cell, CD8+IL-17+ T cell, CD4+ Foxp3+ T, CD8+ Foxp3+ T cell;Serum levels of inflammatory cytokines;Serum antibody level;Ovarian growth factor;

Countries

China

Contacts

Public ContactShaorong Gao

First Maternity and Infant Hospital Affiliated to Tongji University

gaoshaorong@tongji.edu.cn+86 021-65985182

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026