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Clinical study using autologous stromal vascular fraction (mSVF) separated by micropore method including autologous platelet-rich plasma in patients with premature ovarian failure

Clinical study using autologous stromal vascular fraction (mSVF) separated by micropore method including autologous platelet-rich plasma in patients with premature ovarian failure

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0010350
Enrollment
10
Registered
2025-03-28
Start date
2025-04-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

None listed

Interventions

Others(Autologous fat mechanical stromal vascular fraction (mSVF) separated by micropore method including autologous platelet-rich plasma) : Separate mSVF from autologous fat and directly inject appro

Sponsors

Sinsoe Women's Clinic
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: 1. Women aged 20 to 40 years with a need for childbirth 2. Patients diagnosed with premature ovarian failure with a serum level of follicle-stimulating hormone (FSH) of 25 mlU/mL or higher 3. Patients with a serum level of anti-Müllerian hormone (AMH) of 1.1 ng/mL or lower 4. Menstrual cessation or menorrhagia for at least 4 months 5. Women with a uterus and bilateral adnexa 6. Those who voluntarily participated in the study after receiving a sufficient explanation of the study

Exclusion criteria

Exclusion criteria: 1. Women with autoimmune diseases 2. Women with severe diseases that make pregnancy unsuitable, such as diseases of the circulatory, urinary, digestive, endocrine, respiratory, or immune systems 3. Women who have continuously used systemic glucocorticoids or other immunosuppressants for more than 3 weeks within 6 months 4. Women with a history of malignancy, radiotherapy, or chemotherapy 5. Those who are confirmed to be pregnant or breastfeeding 6. Those registered in other clinical studies and trials 7. Those deemed unsuitable by other investigators

Design outcomes

Primary

MeasureTime frame
Adverse Events

Secondary

MeasureTime frame
Blood hormone test (AMH, FSH, LH, E2);Bone Mineral Density (BMD)

Countries

Korea, Republic of

Contacts

Public ContactJAE YOUNG CHO

Sinsoe Women's Clinic

cjy3549@naver.com+82-2-3453-5719

Outcome results

None listed

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