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The incidence, risk factors and clinical outcome of cytomegalovirus reactivation in patients with sepsis-related ARDS

The incidence, risk factors and clinical outcome of cytomegalovirus reactivation in patients with sepsis-related ARDS

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2000033688
Enrollment
Unknown
Registered
2020-06-09
Start date
2020-07-01
Completion date
Unknown
Last updated
2020-08-31

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

Conditions

Respiratory and Critical Medicine

Interventions

HCMV reactivation group:Nil
HCMV non-reactivation group:Nil

Sponsors

The First Affiliated Hospital of Guangzhou Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: (1) Meets the diagnostic criteria for sepsis; (2) Meets the ARDS diagnostic criteria; (3) Sign informed consent; (4) Aged >=18 years.

Exclusion criteria

Exclusion criteria: (1) Patients who are pregnant or lactating; (2) Serum HCMV serology (HCMV IgG) negative; (3) HCMV reactivation already exists at the time of transfer; (4) Expected survival time < 72h; (5) Antiviral drugs used before transfer to ICU; (6) Neutropenia (total leukocytes <1000/µL or neutrophils <500/µL) in ICU).

Design outcomes

Primary

MeasureTime frame
Laboratory-related indicators;Clinically relevant indicators;HCMV DNA;Positive rate of HCMV IgG;

Countries

China

Contacts

Public ContactZhihui Zhang

The First Affiliated Hospital of Guangzhou Medical University

pspaii@sina.com+86 13533102092

Outcome results

None listed

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