Severe Dengue

3

Review clinical trials related to Severe Dengue. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Efficacy of Dengue Infection With Warning Signs Treated With Dexamethasone (DengDex Study)

The goal of this randomized double-blinded placebo-controlled trial is to learn about dexamethasone and the treatment of severe dengue population. The main question it aims to answer are steroid therapy may be effective in dengue.

Participants needed: 200
Trial details
Age: 7-99Biological sex: AllType: InterventionalSponsor: Chulalongkorn UniversityUpdated: Jun 16, 2026Locations: 2
Eligibility criteria

Laboratory confirmed Dengue infected patients (Positive NS1 Ag or anti-DENV IgM... [+5]

Severe dengue> 24 hrs [+3]

Status: Not yet recruiting

Therapeutics for Moderate and Severe Dengue

The purpose of this multi-site, factorial randomised, platform trial is to evaluate host-directed therapeutic agents in patients hospitalised with moderate and severe dengue virus infection. Our primary aim is to find safe and affordable therapeutics which prevent disease progression among those at high risk for severe dengue, and improve outcomes for those with established severe disease, thereby also reducing the substantial burden placed on health systems in dengue endemic regions.

Participants needed: 8,800
Trial details
Phase: Phase 3Age: 5+Biological sex: AllType: InterventionalSponsor: Oxford University Clinical Research Unit, VietnamUpdated: Apr 21, 2026Locations: 18
Eligibility criteria

Age ≥5 years [+14]

Patients on ≥ day 10 of illness or who are clinically improving in the opinion o... [+1]

Status: Recruiting

Innovative Multidisciplinary Strategies for Combating Severe Dengue

The goal of this observational study is to identify biomarkers and host factors associated with dengue severity in patients from dengue-endemic regions. The main question it aims to answer is: Can multi-omics approaches predict disease severity and identify key factors contributing to severe dengue infections? Participants will include individuals with dengue infection, and the study will analyze their blood samples using multi-omics techniques to uncover host immune responses, disease pathogenesis, and cellular pathway interactions. The study will also assess the role of primary and secondary infections, virus serotypes, and immunological factors in disease progression. Findings aim to support disease management, improve severity prediction, and identify potential therapeutic targets to prevent severe outcomes.

Participants needed: 1,400
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Karolinska InstitutetUpdated: Feb 10, 2025Locations: 2
Eligibility criteria

Myalgia, arthralgia [+16]