Evidence map›Paper›PMID 42247469›Full record

SynthesisPLoS neglected tropical diseases2026

A systematic mapping review of therapeutic clinical trials in dengue.

Tran Bang Huyen, Angela McBride, Tun-Linn Thein, Khoi Minh Le, Tran Luu, Nguyen Quang Huy, Eli Harriss, Matthew J W Kain, Jonathan Cattrall, Caitlin Naylor and 7 more

Abstract readSystematic Review
In one paragraph

Synthesis in PLoS neglected tropical diseases, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Tran Bang HuyenOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.ORCID https://orcid.org/0009-0002-1916-2678
Angela McBridePandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Tun-Linn TheinNational Centre for Infectious Diseases, Singapore, Singapore.
Khoi Minh LeOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Tran LuuOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Nguyen Quang HuyOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Eli HarrissBodleian Healthcare Libraries, University of Oxford, Oxford, United Kingdom.
Matthew J W KainInstitute of Naval Medicine, Gosport, United Kingdom.
Jonathan CattrallPandemic Sciences Institute, University of Oxford, Oxford, United Kingdom.
Caitlin NaylorNuffield Department of Medicine, Centre of Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom.
Ho Quang ChanhOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Nguyen Lam VuongOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.
Daniel MunblitKings College London, London, United Kingdom.
Po-Ying ChiaNational Centre for Infectious Diseases, Singapore, Singapore.
Phung Khanh LamNational University of Singapore, Singapore, Singapore.
James A WatsonNuffield Department of Medicine, Centre of Tropical Medicine and Global Health, University of Oxford, Oxford, United Kingdom.
Sophie YacoubOxford University Clinical Research Unit, Ho Chi Minh City, Vietnam.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDengue is a growing public health threat with increasing case numbers globally. Despite the substantial burden, there are no licensed therapeutics for patients with dengue. To inform the design of large-scale practice-changing clinical trials and to assess the feasibility of an individual patient data platform for meta-analysis, we conducted a systematic mapping review of clinical trials evaluating dengue therapeutics. Our aims were to characterise published and registered dengue therapeutic trials, describe their endpoints, and assess study design quality and internal validity to inform feasibility of meta-analysis and future research.

methodsWe systematically searched Ovid MEDLINE, Ovid EMBASE, WHO ICTRP and ClinicalTrials.gov for prospective clinical trials evaluating therapeutics in patients with symptomatic dengue. Two independent reviewers screened records using Covidence. Data were extracted into a REDCap database, and risk of bias was assessed using the ROB-2 and ROBINS-I tools to describe trial design rigour. Descriptive analyses summarised the interventions, trial characteristics, study populations, and primary endpoints. This systematic review was pre-registered with PROSPERO (CRD42023469022). RESULTS & DISCUSSION: A total of 121 clinical studies were identified, comprising 72 published trials and 49 registered but unpublished studies. Interventions were categorised according to the authors' proposed mechanism of action: antiviral (n = 10), host-directed (HDT, n = 34), supportive (n = 31), or undefined (n = 46). Aside from the studies of supportive therapies (n = 31) and unpublished studies (n = 37) which were only reviewed for their primary outcomes, 53 publications remained for review of therapeutic efficacy. Methodological concerns were common - 24 of 53 published trials (45%) were classified as having high or critical risk of bias. Corticosteroids were the most frequently evaluated intervention, involving a total of 944 randomised patients. The primary endpoints used in both antiviral and HDT trials were highly heterogeneous, limiting comparability. The combination of methodological concerns and non-standardised endpoints precluded meta-analysis for any intervention. No single treatment had sufficient or consistent evidence to support recommendations for use in clinical practice.

conclusionsOur findings highlight a remarkably sparse evidence base for dengue therapeutics and a lack of standardised, clinically meaningful endpoints. These factors have hindered progress in evaluating candidate treatments and limited the potential for individual patient data meta-analyses. Large, high-quality trials - powered for harmonised and clinically relevant endpoints - are urgently needed to advance the development of effective therapies for dengue.

Indexed as

Clinical Trials as TopicDengueAntiviral AgentsHumansAntiviral Agents

Identifiers

PMID42247469
PMCPMC13241016

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.