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Rapid Diagnostic Tests and Clinical/Laboratory Predictors of Tropical Diseases In Patients With Persistent Fever in Cambodia, Nepal, Democratic Republic of the Congo and Sudan (NIDIAG-Fever)

University Hospitals (UH) logo

University Hospitals (UH)

Status

Completed

Conditions

Brucellosis
Relapsing Fever
Rickettsial Diseases
Visceral Leishmaniasis
Melioidosis
Tuberculosis
HIV
Malaria
Leptospirosis
Enteric Fever
Amoebic Liver Abscess
Human African Trypanosomiasis

Treatments

Device: Test-it Typhoid IgM
Device: Card Agglutination Trypanosoma Test (CATT)-10
Device: Immunochromatographic HAT test
Device: S. typhi IgM/IgG
Device: HAT Serostrip
Device: IT LEISH (rK39)
Device: Test-it Leptospirosis IgM
Device: rk28 ICT
Device: Leptospira IgG/IgM
Device: Typhidot M

Study type

Interventional

Funder types

Other

Identifiers

NCT01766830
260260 (Other Grant/Funding Number)
WP2-01-FEV

Details and patient eligibility

About

Tropical fevers have been a diagnostic challenge from the antiquity. Nowadays, despite the availability of good diagnostic capacities, undifferentiated febrile illnesses continue to be a thorny problem for travel physicians. In developing countries, the scarcity of skilled personnel and adequate laboratory facilities makes the differential diagnosis of fevers even more complex. Health care workers must often rely on syndrome-oriented empirical approaches to treatment and might overestimate or underestimate the likelihood of certain diseases. For instance Neglected Tropical Diseases (NTD) contribute substantially to the burden of persistent (more than 1 week) fevers in the Tropics, causing considerable mortality and major disability. These diseases are however rarely diagnosed at primary health care (PHC) level. The difficulty in establishing the cause of febrile illnesses has resulted in omission or delays in treatment, irrational prescriptions with polytherapy, increasing cost and development of drug resistance.

In resource-limited settings, clinical algorithms constitute a valuable aid to health workers, as they facilitate the therapeutic decision in the absence of good laboratory capacities. There is a critical lack of appropriate diagnostic tools to guide treatment of NTDs. While clinical algorithms have been developed for some NTDs, in most cases they remain empirical. Besides, they rarely take into account local prevalence data, do not adequately represent the spectrum of patients and differential diagnosis at the primary care level and often have not been properly validated. The purpose of the study is to develop evidence-based Rapid Diagnostic Test (RDT)-supported diagnostic guidelines for patients with persistent fever (≥ 1 week) in the Democratic Republic of the Congo (DRC), Sudan, Cambodia and Nepal.

Full description

This study is part of a large European Union (EU)-funded research project called NIDIAG that aims at developing integrated, evidence-based syndromic approach to improve management of NTD-related clinical syndromes. NIDIAG targets three non-specific clinical syndromes: the persistent fever, neurological, and intestinal syndrome. The objective of the project is to establish diagnostic guidelines for each of this syndrome, with a particular focus on severe and treatable neglected infectious diseases. The developed guidelines should integrate relevant Point-of-Care (POC)tests.

The persistent fever syndrome targeted by NIDIAG is defined as presence of fever for at least one week. The list of diseases - both NTD and other Infectious Diseases (ID) - that frequently cause persistent (≥1 week) fever in the study countries includes: Visceral Leishmaniasis (VL), Human Africa Trypanosomiasis (HAT), Enteric (typhoid, paratyphoid) fever, Malaria, Brucellosis, Melioidosis, Tuberculosis, Amoebic liver abscess, Relapsing fever, HIV, Rickettsial diseases, and Leptospirosis. The study will try to identify clinical and laboratory predictors of these diseases as well as validate existing RDTs.

Enrollment

1,927 patients

Sex

All

Ages

5+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • fever for ≥ 1 week
  • ≥ 5 years old (18 years onward in Cambodia)

Exclusion criteria

  • unwilling or unable to give written informed consent
  • unable in the study physician's opinion to comply with the study requirements
  • existing laboratory confirmed diagnosis
  • need of immediate intensive care due to shock or respiratory distress

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

1,927 participants in 1 patient group

Phase 3 Diagnostic
Experimental group
Description:
A total of 10 RDTs will be assessed in the patients cohort for the respective target condition
Treatment:
Device: Card Agglutination Trypanosoma Test (CATT)-10
Device: Immunochromatographic HAT test
Device: Leptospira IgG/IgM
Device: Test-it Leptospirosis IgM
Device: rk28 ICT
Device: S. typhi IgM/IgG
Device: Typhidot M
Device: HAT Serostrip
Device: Test-it Typhoid IgM
Device: IT LEISH (rK39)

Trial contacts and locations

7

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Data sourced from clinicaltrials.gov

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