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Foscarnet sodium for the treatment of pure erythrocyte aplastic anemia due to parvovirus B19 infection after kidney transplantation:study protocol for a prospective single-center trial

Foscarnet sodium for the treatment of pure erythrocyte aplastic anemia due to parvovirus B19 infection after kidney transplantation:study protocol for a prospective single-center trial

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000031933
Enrollment
Unknown
Registered
2020-04-15
Start date
2020-04-14
Completion date
Unknown
Last updated
2020-04-20

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

Conditions

Pure red blood cell aplastic anemia after kidney transplant

Interventions

case series:Foscarnet ( IV.)

Sponsors

The First Affiliated Hospital of Zhejiang University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Voluntary informed consent, any age and gender; (2) Intractable moderate to severe anaemia after kidney transplantation; (3) qPCR positive for microbial B19 virus nucleic acid; (4) Hemoglobin <100g/L and reticulocytes <0.5%; (5) Patients routinely taking triple antiimmune drugs after surgery; (6) Preoperative population-reactive antibody (PRA) negative, no fever and significant anaemia; (7) All donor and recipient HBV-DNA, CMV-IgG, CMV-IgM, CMV-DNA, HIV- IgG and syphilis tests were negative; (8) All transplants were successful and postoperative renal function was well restored; (9) The ability of the patient to follow the study protocol as determined by the investigator.

Exclusion criteria

Exclusion criteria: (1) An allergic body with a known allergy to sodium phosphonate or 2 or more other drugs or foods used by injection; (2) Multi-organ transplant, multiple transplants; (3) Loss of early transplanted kidneys; (4) Moderate and severe anaemia due to surgical bleeding, bone marrow suppression, hematologic disorders, etc.; (5) Pregnant or lactating women; (6) In the judgment of the investigator, there are other factors that may cause the subject to be forced to discontinue the study, such as other serious illnesses, serious laboratory abnormalities, other factors that affect the safety of the subject or the collection of test information and blood samples.

Design outcomes

Primary

MeasureTime frame
hemoglobin;

Secondary

MeasureTime frame
virus copy number;reticulocyte;blood creatinine;

Countries

China

Contacts

Public ContactPENG WENHAN

The First Affiliated Hospital of Zhejiang University School of Medicine

pengwenhan2005@sina.com+86 13515710415

Outcome results

None listed

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