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Clinical study of human umbilical cord mesenchymal stem cell-derived apoptotic vesicles (MSC-apoVs) in the treatment of premature ovarian insufficiency

Clinical study of human umbilical cord mesenchymal stem cell-derived apoptotic vesicles (MSC-apoVs) in the treatment of premature ovarian insufficiency

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500097317
Enrollment
Unknown
Registered
2025-02-17
Start date
2025-02-17
Completion date
Unknown
Last updated
2025-02-24

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

Conditions

Premature Ovarian Insufficiency

Interventions

treatment group:Local single injection of human umbilical cord mesenchymal stem cell apoptotic vesicles (MSC-apoVs) on both ovaries

Sponsors

The Second People’s Hospital of Foshan
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1.Age >=18 years old; 2.Patients with newly diagnosed POI who refused hormone replacement and voluntarily chose to participate in this study; 3.Patients who have been diagnosed with POI and have poor clinical treatment effect; 4.Sign the subject's informed consent.

Exclusion criteria

Exclusion criteria: 1.There are genetic factors associated with ovarian reserve deficiency (Turner syndrome, chromosome abnormalities, etc.); 2.untreated submucous fibroids, untreated endometrial polyps, uterine adhesions, untreated pathological ovarian cysts, and previous ovaria-related surgical history; 3.Patients with severe or unstable cardiovascular, respiratory, liver, kidney, blood, endocrine, central nervous system, immune dysfunction and malignant tumor diseases; 4.Acute and chronic pelvic inflammation and suspected pelvic adhesion; 5.Patients with relevant hormone replacement therapy 3 months before screening; 6.Hepatitis B, hepatitis C activity period; 7.Patients who have been diagnosed with hyperthyroidism or hypothyroidism within one year before screening and are still taking medication; 8.Those who have plans to have a second child or plan to get pregnant in the near future; 9.The investigator believes that the subjects have other conditions that are not suitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Safety evaluation index;

Secondary

MeasureTime frame
Effectiveness evaluation index;

Countries

China

Contacts

Public ContactDong Julang

The Second People’s Hospital of Foshan

1041616157@qq.com+86 757 88032005

Outcome results

None listed

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