Skip to content

The Tolerance Test of Single Dose Treatment of Thrombocytopenia with "Injection of Umbilical Cord Blood Megakaryocyte Progenitor Cells" after Radiotherapy and Chemotherapy.

The Tolerance Test of Single Dose Treatment of Thrombocytopenia with "Injection of Umbilical Cord Blood Megakaryocyte Progenitor Cells" after Radiotherapy and Chemotherapy.

Status
Active, not recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-TCH-09000333
Enrollment
Unknown
Registered
2009-02-18
Start date
2008-12-09
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

thrombocytopenia after radiotherapy and chemotherapy

Interventions

Treatment group:thrombocytopenia with “Injection of Megakaryocyte Progenitor Cells from Umbilical Cord Blood” after radiotherapy and chemotherapy.

Sponsors

Institute of Transfusion Medicine, The Academy of Military Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Aged from 18 to 70 years old, open to men and women; 2. within one month after cancer radiotherapy and chemotherapy; 3. ECOG grades 0 or 1, expected survival time is more than or equal to three months; 4. Subjects are thrombocytopenia patients caused by cancer radiotherapy and chemotherapy; 5. platelet, which is more than 20*10^9/L and less than 50*10^9/L; 6. Results of liver and renal function are in normal or basic normal situation; 7. There is no infusion contraindication about injection of umbilical cord blood megakaryocyte progenitor cells; 8. understand and sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. thrombocytopenia without cancer radiotherapy and chemotherapy; 2. Sternum or pelvis had received radiotherapy; 3. Patients with primary disease in important organs(liver, kidney), patients accompanied by the immune system disease, serious infections, mental disorders or organ transplant recipients; 4. pregnant, breast-feeding women; 5. Patients did not sign informed consent form; 6. infusion contraindication about injection of umbilical cord blood megakaryocyte progenitor cells.

Design outcomes

Primary

MeasureTime frame
The time and response to platelet increasing;

Countries

China

Contacts

Public ContactPei Xuetao
peixt@nic.bmi.ac.cn+86 010 66932240

Outcome results

None listed

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