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The Efficacy of Hemoperfusion Therapy in Patients with Dengue Shock Syndrome

The Efficacy of Hemoperfusion Therapy in Patients with Dengue Shock Syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20250513003
Enrollment
96
Registered
2025-05-13
Start date
2025-05-15
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Dengue shock syndrome patients admitted to the Intensive Care Units Cytokine storm, Dengue, Dengue shock syndrome, Hemoperfusion

Interventions

Patient receiving hemoperfusion treatment,Patient not receiving hemoperfusion treatment
Treatment,Treatment

Sponsors

Faculty of Medicine, Chiang Mai University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age at least 20 years old with confirm dengue infection by one of the following methods; Dengue NS1Ag, Anti DENV-IgM/IgG, or PCR for Dengue 2. Diagnosed as severe Dengue (DHF grade III/IV, DSS) with evidence of plasma leakage - Hematocrit rising at least 20% or evidence of fluid accumulation (according to DHF grade III/IV classification of WHO, 2011 SEARO) and clinical include severe bleeding, severe organ involvement (acute hepatitis, acute liver failure, acute kidney injury, myocarditis, encephalitis) 3. Multiorgan failure (more than 2 organ e.g. Respiratory failure, Liver failure, or Renal failure) 4. Admitted in ICU at Chiang Mai University Hospital Chiang Mai, Thailand

Exclusion criteria

Exclusion criteria: 1. Pregnancy 2. Known case ESRD 3. Malignancy with on Immunotherapy 4. Limited performance status (ECOG at least 3) 5. Incomplete data collection (50% of data) specifically SOFA, APACHE-II score, serum creatinine, CBC, lactate, hs-CRP

Design outcomes

Primary

MeasureTime frame
Severity score 1 month Sequential organ failure assessment (SOFA) score

Secondary

MeasureTime frame
Patient outcomes 1 month Mortality, inflammatory cytokines (lactate, hs-CRP), liver function test, renal function test, and the need for long-term hemodialysis

Countries

Thailand

Contacts

Public ContactPrit Kusirisin

Faculty of Medicine, Chiang Mai University

jingprit@hotmail.com053936452

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026