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Halploidentical hematopoietic stem cell transplant by intra-bone injection for patients with hematologic malignances

Halploidentical hematopoietic stem cell transplant by intra-bone injection for patients with hematologic malignances

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IPR-15005794
Enrollment
Unknown
Registered
2015-01-07
Start date
2015-03-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

malignant hematologic disorders

Interventions

intra-bone injectioin:Intra-bone injection of mononuclear cells from bone marrow
transfusion by venous:transfuse the hematopietic cells by venous

Sponsors

Central South University Xiangya Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: At the age of 14 years old to 65 years old (14 years old and 65 years old); According to the classification standard of diagnosis of malignant diseases of the blood system in 2008 edition of WHO, MDS and leukemia patients; With hematopoietic stem cell transplantation indications but no HLA matched sibling or unrelated donor transplantation; or the condition requirements as soon as possible without looking HLA haploidentical donor opportunity; The last time to start of chemotherapy into the group of at least 30 days; the last time to the end of chemotherapy into the group of at least 10 days; The specificity of HCT prognostic index (HCT-CT) of less than 4 (including 4); Cardiac ejection fraction greater than 50% (including 50%); The total bilirubin level in the normal 2 times the upper limit of the following; alanine aminotransferase and aspartate aminotransferase levels in the normal 3 times the upper limit of the following; Diffusion capacity for carbon monoxide (according to hemoglobin level adjusted) greater than 40% (including 40%); forced expiratory volume in one second more than 50% (including 50%); Creatinine clearance rate greater than 50ml/min; Signed informed consent.

Exclusion criteria

Exclusion criteria: Symptoms of coronary heart disease; In group 4 weeks before the memory in the central nervous system leukemia (primitive cells in cerebrospinal fluid of positive); The fitness score less than 70 points; Viruses, bacteria and fungi uncontrolled infection (Advances in antifungal therapy process still condition); HIV seropositive; Other system malignant tumor history; Pregnant and lactating women; Do not agree in the trial period and male and female contraception;

Design outcomes

Primary

MeasureTime frame
survival time;disease free survival time;

Secondary

MeasureTime frame
Death associated with transplant;incidence and degree of graft-versus-host disease;

Countries

China

Contacts

Public ContactBin Fu
xyfubin@126.com+86 13755006662

Outcome results

None listed

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