Skip to content

High-dose intravenous immunoglobulin therapy for refractory viral infection after allogeneic hematopoietic stem cell transplantation.

High-dose intravenous immunoglobulin therapy for refractory viral infection after allogeneic hematopoietic stem cell transplantation. - High-dose intravenous immunoglobulin therapy for refractory viral infection after allogeneic hematopoietic stem cell transplantation.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000003034
Enrollment
14
Registered
2010-01-14
Start date
2010-02-19
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Refractory viremia with high viral load, viral infection and viral disease after allogeneic hematopoietic stem cell transplantation

Interventions

Intravenous immunoglobulin(400mg/kg/day) for 5 days.

Sponsors

Hematology, Osaka City University, Graduate School of Meicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with hematological disease who received allogeneic hematopietic stem cell transplantation and meet the following criteria. 1) Ganciclovir or foscavir-resistant CMV infection or disease. 2) Aciclovir or valaciclovir-resistant HSV, VZV infection or disease. 3) Refractory adenovirus-associated hemorrhagic cystitis 4) Viral pneumonia 5) Viral gastroenteritis 6) Viral hepatitis 7) Viral encephalitis and meningitis 8) The following viremias with clinical symptom [1]EBV [2]HHV-6 [3]ADV [4]Ganciclovir or foscavir-resistant CMV viremia [5]Aciclovir or valaciclovir-resistant HSV, VZV viremia [6]parvovirus B19

Exclusion criteria

Exclusion criteria: 1) History of allergic reaction to immunoglobulin preparations 2) History of severe adverse effect of immunoglobulin preparations 3) Presence of veno-occlusive disease (VOD) after allogeneic stem cell transplantation 4) Positivity of HIV-antibody, HCV-antibody, HBs-antigen, or HBV-DNA 5) No indication for this study judged by physician in charge

Design outcomes

Primary

MeasureTime frame
Cure rate of viremia and virus disease

Secondary

MeasureTime frame
1)Reduction of viral load 2)Degree of improvement in clinical symptoms, imaging findings and clinical laboratory test results

Countries

Japan

Contacts

Public ContactMika Nakamae

Osaka City University, Graduate School of Medicine Hematology(Clinical center for hematological malignancies )

crc-hematology@med.osaka-cu.ac.jp06-6645-3881

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026