Skip to content

Clinical Study of Intensive Immunoablative conditioning regimen on Umbilical Cord Blood Transplantation Related Diseases

Clinical Study of Intensive Immunoablative conditioning for Umbilical Cord Blood Transplantation in Treating Related Diseases

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800014708
Enrollment
Unknown
Registered
2018-01-30
Start date
2013-10-01
Completion date
Unknown
Last updated
2020-02-10

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

Conditions

malignant and nonmalignant hematological disease

Interventions

Case series:Busulfan+Cyclophosphamide+Fludarabine conditioning regimen

Sponsors

ZhongDa Hospital Southeast University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
0.5 Years to 30 Years

Inclusion criteria

Inclusion criteria: (1) aged 2.5x10^7/kg and CD34 cell dose >1.2x10^5/kg; if the cell dose was insufficient with a single CBU, double cord blood unit was used; (4) the score of Karnofsky >=80; (5) Signed written informed consent.

Exclusion criteria

Exclusion criteria: (1) Serious viscera dysfunction or disease, such as serious diseases and function disorder in heart, liver, kidney and pancreas; (2) Patients with pregnancy; (3) Participants and/or authorized family members refused to accept UCBT; (4) Researchers believe that can damage the unnecessary risks to safety, make the results of the study subjects any life-threatening illness, condition or organ system dysfunction; drug dependence; uncontrolled mental disease; cognitive impairment; (5) Researchers think that the patient doesn't fit into the study.

Design outcomes

Primary

MeasureTime frame
Cumulative rate of neutrophil engraftment;Cumulative rate of platelet engraftment;Overall survival;GVHD;chimerism;relapse;

Countries

China

Contacts

Public ContactDing Jiahua

Zhongda Hospital Southeast University

101007972@seu.edu.cn+86 13809027048

Outcome results

None listed

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