Clinical Trials Directory

Trials / Unknown

UnknownNCT04422782

New Tools for Predicting Capillary Leak Shock During Dengue Fever

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
342 (estimated)
Sponsor
Centre Hospitalier de Cayenne · Academic / Other
Sex
All
Age
5 Years
Healthy volunteers
Not accepted

Summary

Evaluate the prognostic value of different methods (Osmometry / clinical-biological score) compared to the occurrence of capillary leak shock during dengue fever.

Detailed description

On the South American continent, dengue fever progressively progresses to hyperendemia with co-circulation of different serotypes. Among the complications of dengue fever, a frequent complication is the shock linked to capillary leakage which often occurs at the time of defervescence between the 3rd or 5th day of evolution of the fever. Before that, it is difficult to identify patients who are at risk for severe forms. Patients are therefore seen regularly to monitor for the development of serious forms, which causes saturation of the health system. Despite everything, with each epidemic, the investigators observe deaths of previously healthy people, which always constitutes an important trauma for the population and for the carers. Improving the understanding of the pathophysiology of capillary leakage and the tools to predict it would be significant advances in this common tropical pathology. Thus a retrospective study of longitudinal data during the dengue 2 epidemic of 2013 made it possible to generate precise hypotheses as to the pathophysiology of the shock linked to capillary leakage. Hypoprotidemia and hyponatremia having a strong statistical association with the subsequent occurrence of shock, the hypothesis is of a progressive disturbance of the plasma osmolarity resulting in water leaks towards the interstitial sector. These preliminary data also made it possible to develop a predictive score which must now be validated over time. Research involving the human person, monocentric, prospective, validation Interventional research protocol involving the human person category 2 at risk and minimal constraints

Conditions

Interventions

TypeNameDescription
OTHERFor each routine sample, an additional tube will be collected to measure the osmotic pressure in the blood and urineInterventional research protocol involving the human person category 2 at risk and minimal constraints

Timeline

Start date
2020-05-14
Primary completion
2022-05-14
Completion
2023-05-14
First posted
2020-06-09
Last updated
2020-12-10

Locations

1 site across 1 country: France

Source: ClinicalTrials.gov record NCT04422782. Inclusion in this directory is not an endorsement.