Skip to content

Clinical study for umbilical cord blood mesenchymal stem cells combined with peripheral blood stem cells co-transplantation with reduced PT-Cy in the prevention of GVHD in the treatment of aplastic anemia

Clinical study for umbilical cord blood mesenchymal stem cells combined with peripheral blood stem cell co-transplantation with reduced PT-Cy in the prevention of GVHD in the treatment of aplastic anemia--single-center, single-arm, open clinical study

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900026462
Enrollment
Unknown
Registered
2019-10-11
Start date
2019-08-19
Completion date
Unknown
Last updated
2019-10-14

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

Conditions

aplastic anemia,AA

Interventions

Cass series:low dose post Cyclophosphamide and Mesenchymal stem cell

Sponsors

Cancer Hospital Affiliated to Zhengzhou University-He'nan Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Aged 14 to 50 years old; 2. ECOG score < 2 (Appendix 2); 3. AA was diagnosed by definite blood routine, reticulocyte count, multi-site bone marrow puncture and bone marrow biopsy. 4. At present, patients have no other effective treatment, or patients choose allo-HSCT voluntarily. 5. The main organs and tissues of the patients have good functions: (1) cardiac function: without heart disease or coronary heart disease, the heart function of the patients is grade 1-2 (Appendix 3); (2) liver function: TBIL < 3ULN, AST < 2.5ULN, ALT < 2.5ULN; (3) renal function: Cr < 1.25ULN; 6. The peripheral superficial venous blood passage of the patient is unobstructed, which can meet the needs of intravenous drip. 7. The patient himself agreed to participate in the clinical study and signed the Informed Consent Form.

Exclusion criteria

Exclusion criteria: 1. Systemic active infections requiring treatment; 2. suffer from serious heart, liver, kidney dysfunction and other diseases; 3. HIV infected patients; 4. suffering from serious autoimmune diseases or immunodeficiency diseases; 5. Severe allergic constitution; 6. Severe mental disorders; 7. Other clinical trial researchers who have participated in or are currently participating in the past three months; 8. With other serious diseases (such as autoimmune diseases and immunodeficiency) that conflict with this program; 9. With history of other malignant tumors.

Design outcomes

Primary

MeasureTime frame
Routine blood test;Osseous puncture;electrocardiogram;Color Doppler ultrasound;CT;Biochemical indicators;

Countries

China

Contacts

Public ContactZhou Jian

Cancer Hospital Affiliated to Zhengzhou University-He'nan Cancer Hospital

zhoujiandoctor@163.com+86 13623822347

Outcome results

None listed

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