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Retrospective analysis of cytomegalovirus retinitis after bone marrow transplantation

Retrospective analysis of cytomegalovirus retinitis after bone marrow transplantation

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300077237
Enrollment
Unknown
Registered
2023-11-02
Start date
2023-11-02
Completion date
Unknown
Last updated
2023-11-06

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

Conditions

cytomegalovirus retinitis after bone marrow transplantation

Interventions

Case series:none

Sponsors

The Second Hospital of Dalian Medical University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? Patients who received allogeneic hematopoietic stem cell transplantation (allo-HSCT) due to any potential malignant hematological disease or non-malignant diseases, and were at least 18 years old at the time of allo-HSCT. ? Patients who were clinically diagnosed with Cytomegalovirus Retinitis (CMVR) based on clinical symptoms and ophthalmological examination. ? Patients who had aqueous humor samples sent for CMV nucleic acid testing and inflammatory factor detection. ? Patients who received ophthalmological or internal antiviral treatment for CMVR after allo-HSCT, and had a treatment plan and follow-up records. ? Patients who had complete medical records, including pre-transplant evaluation, transplant details, and post-transplant follow-up data.

Exclusion criteria

Exclusion criteria: ? Patients who had a history of CMVR prior to receiving allo-HSCT. ? Patients with concurrent eye infections or inflammations that might interfere with the accurate diagnosis and treatment of CMVR. ? Patients who received non-allogeneic stem cell transplantation (such as autologous or syngeneic transplant). ? Patients who did not receive any antiviral treatment for CMVR after allo-HSCT. ? Patients whose medical records were incomplete or missing, impacting the accurate evaluation of research objectives

Design outcomes

Primary

MeasureTime frame
Immunosuppressive therapy used;Viral serological tests and viral load levels;

Secondary

MeasureTime frame
Donor type;Presence of GVHD;

Countries

China

Contacts

Public ContactLiu Fei

The Second Hospital of Dalian Medical University

drliufei@dmu.edu.cn+86 177 0987 2593

Outcome results

None listed

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