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The clinical study of human umbilical cord mesenchymal stem cells in treating patients with thin endometrial infertility

The clinical study of human umbilical cord mesenchymal stem cells in treating patients with thin endometrial infertility

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039890
Enrollment
Unknown
Registered
2020-11-13
Start date
2020-11-16
Completion date
Unknown
Last updated
2021-02-22

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

Conditions

thin endometrial infertility

Interventions

Stem cells combined with collagen scaffolds transplantation group:Stem cells combined with collagen scaffolds transplantation
collagen scaffold transplant group:collagen scaffold transplant

Sponsors

Xiangya Hospital, Central South University
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: (1) 20 to 39 years of age,primary or secondary infertility undergoing in vitro fertilization embryo transfer, >=4 high-quality frozen embryos (defined as 7-9c/II 0 or blastocysts of 4BC and above) and of which >= 2 grade I embryos or blastocysts of 4BC and above; (2) Diagnosed as grade III or higher (according to the 1997 European Gynecological Endoscopy Associations uterine adhesion classification standard) or score > 8 points (according to the 1988 American Reproductive Association uterine adhesion standard) by hysteroscopy, and intrauterine adhesiolysis have been performed, re-examination of hysteroscopy showed normal uterine cavity morphology, and with a score of 4mg/day, the maximum dose is 8mg/day and above), and the endometrial thickness after treatment is less than 7mm; (4) 18kg/m2< BMI < 24 kg/m2; (5) Cov-19 nucleic acid test negative; (6) Those who voluntarily participate and sign the informed consent.

Exclusion criteria

Exclusion criteria: (1) Those who have not been cured of sexually transmitted diseases. (2) those who participate in other clinical researchers in the past three months. (3) those who were positive in serum pregnancy test. (4) patients with coagulation dysfunction or other blood system diseases. (5) patients with severe heart disease, unstable angina pectoris, cardiac insufficiency above III grade, acute myocardial infarction and / or old myocardial infarction, diagnosed as hypertension according to the 2010 Chinese guidelines for the prevention and treatment of hypertension. (6) patients with active genital tuberculosis. (7) patients with immune system diseases. (8) any disease that affect pregnancy outcome: untreated hydrosalpinx, untreated uterine polyps, untreated uterine infection, III~ IV stage endometriosis, adenomyosis, ovarian cyst > 4cm, uterine myoma diameter > 2cm, multiple myoma, intramural and submucosal myoma, poor healing of cesarean incision, pelvic and abdominal benign tumor > 4cm, pituitary tumors and malignant tumors. (9) abnormal uterine bleeding. (10) patients with severe liver and renal function damage, serum alanine aminotransferase (ALT) and aspartate aminotransferase (AST) were 2.5 times higher than the normal upper limit, serum creatinine (Cr) and urea nitrogen (BUN) were 2 times higher than the normal upper limit. (11) patients who were not suitable to be included.

Design outcomes

Primary

MeasureTime frame
endometrial thickness;clinical pregnancy;biochemical pregnancy;livebirth;endometrial pattern;?Np63;Ki67;estrogen receptor alpha;von Willebrand factor;Menstrual changes;

Countries

China

Contacts

Public ContactLi Yanping

Xiangya Hospital, Central South University

lisayanping@sina.com+86 13607317798

Outcome results

None listed

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