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A randomized controlled study for umbilical cord mesenchymal stem cells in the treatment of ovarian reserve dysfunction

A randomized controlled study for umbilical cord mesenchymal stem cells in the treatment of ovarian reserve dysfunction

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900021330
Enrollment
Unknown
Registered
2019-02-15
Start date
2019-06-01
Completion date
Unknown
Last updated
2019-02-18

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

Conditions

Diminished ovarian reserve

Interventions

Group A (control group):Oral dehydroepiandrosterone
Group B (experimental group):Intravenous infusion of umbilical cord mesenchymal stem cells 50ml

Sponsors

The First People's Hospital of Hefei
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 50 years; 2. Patients with large changes in the basic value of FSH; 3. The FSH/LH ratio is increased by >2 to 3.6; 4. The subject or his or her guardian must sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1. Disease factors: (1) Patient ovary has had an infection 2. Past medical history: (1) Patients with malignant tumors within the past 5 years or currently; (2) The patient has alcohol or drug abuse in the past 6 months; (3) The patient has any potential or current medically-accepted mental illness (which may affect the assessment of the subject); 3. Infection: (1) Uncontrolled bacterial, fungal or viral infections in patients with severe or severe systemic or local infections, especially pulmonary infections; sepsis, persistent bacteremia or meningitis; active tuberculosis, severe acute hepatitis, or other active infectious diseases (Including hepatitis B, hepatitis A, HIV positive patients); 4. Visceral dysfunction: Significant organ failure: (1) Heart ? Patients with severe cardiac dysfunction, such as left ventricular ejection rate < 50%; patients with dysfunction such as right ventricular failure and arrhythmia; ? the presence of uncontrolled high blood pressure or congestive heart failure, active angina requiring nitrate, myocardial infarction or arrhythmia or heart failure requiring active treatment in the past 6 months; (2) Lung ? Patients with pulmonary hypertension; ? Patients with diffuse alveolar hemorrhage and other progressive lung diseases may need to maintain blood oxygen concentration through a mask or other auxiliary machinery; hypoxemia, oxygen saturation < 90%; ? Respiratory failure with restrictive or obstructive pulmonary disease or ventilator support; (3) Liver ? In patients with severe liver dysfunction, alanine aminotransferase (ALT), total bilirubin is more than 3 times the normal maximum value; ? severe hepatic vein occlusive disease (VOD) or sinus obstruction; (4) Kidney: severe renal insufficiency, creatinine is more than 2 times the normal maximum value; creatinine clearance rate < 30 mL / min; 5. Others (1) Patients with known allergies, such as those who are allergic to human albumin, who are allergic to any pharmaceutical reagents required for surgery; (2) Pregnant women or patients planning to become pregnant, breast-feeding patients.

Design outcomes

Primary

MeasureTime frame
Follicle stimulating hormone;Follicle stimulating hormone/luteinizing hormone;

Countries

CHINA

Contacts

Public ContactGao Bin

The First People's Hospital of Hefei

gaobin_3136@163.com+86 13905511671

Outcome results

None listed

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