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Clinical trial of foscarnet and ganciclovir for prevention of cytomegalovirus infection after allogeneic hematopoietic stem cell transplantation

Clinical trial of foscarnet and ganciclovir for prevention of cytomegalovirus infection after allogeneic hematopoietic stem cell transplantation

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-INR-16008283
Enrollment
Unknown
Registered
2016-04-14
Start date
2016-04-01
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

cytomegalovirus infection

Interventions

test group:Receive foscarnet for prevention of cytomegalovirus infection from engraftment to day+60 after transplantation
control group:Receive ganciclovir for prevention of cytomegalovirus infection from engraftment to day+60 after transplantation

Sponsors

Department of hematology,Xinqiao Hospital,Third Military Medical University,Chongqing,China
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 55 Years

Inclusion criteria

Inclusion criteria: 1. Aged 12 to 55 years; 2. Patients undergoing allogeneic hematopoietic stem cell transplantation for hematology diseases; 3. Seronegative for CMV IgM; negative for CMV DNA in blood and urine; 4. Understand and voluntarily sign an informed consent.

Exclusion criteria

Exclusion criteria: 1. Absolute neutrophil count 105umol/L; ALT, AST and total bilirubin> 2 times upper limit of normal value; 3. Ongoing antiviral treatment with acyclovir,ganciclovir or foscarnet; 4. Allergy to foscarnet or ganciclovir; 5. Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
Incidence of CMV infection within 100 days after transplantation;Survival rate within 100 days after transplantation;

Secondary

MeasureTime frame
Incidence of CMV disease within 100 days after transplantation;Incidence of durg-related adverse events;

Countries

China

Contacts

Public ContactXi Zhang

Department of hematology, Xinqiao Hospital, Third Military Medical University

zhangxxi@sina.com+86 13808310064

Outcome results

None listed

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