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Improving Diagnosis of Tuberculosis in HIV Infected Children in Asia (Cambodia, Vietnam)and Africa (Burkina Faso, Cameroon)

Improving Diagnosis of Tuberculosis in HIV Infected Children in Asia (Cambodia, Vietnam) and Africa (Burkina Faso, Cameroon) ANRS 12229 PAANTHER 01 (Pediatric Asian African Network for Tuberculosis and HIV Research)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01331811
Enrollment
441
Registered
2011-04-08
Start date
2011-04-30
Completion date
2014-05-31
Last updated
2015-08-05

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

Conditions

HIV, Pediatrics, Tuberculosis

Keywords

HIV, Tuberculosis, Diagnosis, Pediatrics, Asia, Africa

Brief summary

Childhood tuberculosis (TB) accounts for 11% of the total 9 million annual TB cases and the difficulty of its diagnosis is increased in case of HIV infection in children. The aim of this study is to improve TB diagnosis in HIV-infected children by developing a new diagnostic algorithm incorporating new tools available such as: * interferon gamma release assays (IGRAs), as alternative to the tuberculin skin test * alternative specimen collection methods such as string test (or Enterotest (R)), nasopharyngeal aspirates and stools samples, as alternatives to gastric aspirate * the Xpert MTB/RIF assay

Interventions

OTHERDevelopment of a diagnosis algorithm

At entry in the study, HIV infected children with suspected tuberculosis will undergo a complete evaluation including: * interview on anamnesis * clinical examination * evaluation of HIV infection stage * hematology and biochemistry tests * CD4 count * HIV viral load * IGRA * chest radiograph * Abdominal ultrasonograph to detect abdominal lymphadenopathy * Tuberculin skin test * gastric aspirates, sputum and string tests according to the age of children * nasopharyngeal aspirate * stool sample * lymph node fine needle aspirate or other specimen collection if applicable Diagnosis and treatment of all participating children will be done according to national guidelines. The children will be followed-up for 6 months until the end of their anti-TB treatment. For the analysis of data and the validation of the algorithm, children will be randomized into 2 groups. Data from Group I will be used to develop the algorithm; data from Group II will be used to validate it.

Sponsors

Institut Pasteur, Cambodia
CollaboratorOTHER
National Pediatric Hospital, Cambodia
CollaboratorUNKNOWN
Angkor Hospital for Children
CollaboratorOTHER
Pham Ngoc Thach Hospital, Ho Chi Minh City, Vietnam
CollaboratorOTHER
Pediatric Hospital Nhi Dong 1, Ho Chi Minh City, Vietnam
CollaboratorUNKNOWN
Number 2 Children's Hospital, Ho Chi Minh City
CollaboratorOTHER
Hôpital Necker-Enfants Malades, Paris, France
CollaboratorUNKNOWN
Groupe Hospitalier Pitie-Salpetriere
CollaboratorOTHER
CHRU Arnaud de Villeveuve, Montpellier, France
CollaboratorUNKNOWN
IRD, Yaounde, Cameroon
CollaboratorUNKNOWN
Fondation Chantal Biya,Yaounde, Cameroon
CollaboratorUNKNOWN
CHU Sourô Sanou, Bobo Dioulasso, Burkina Faso
CollaboratorUNKNOWN
Centre Muraz
CollaboratorOTHER
Centre Pasteur du Cameroun
CollaboratorOTHER
Centre Hospitalier D'essos
CollaboratorOTHER
ANRS, Emerging Infectious Diseases
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 13 Years
Healthy volunteers
No

Inclusion criteria

* children aged from 0 to 13 years * confirmed HIV infection * suspicion of tuberculosis * informed consent signed by at least one parent or guardian * on ARVs or not

Exclusion criteria

* history of anti TB treatment started in the past 2 years * on going tuberculosis treatment * Suspicion of exclusive extra-thoracic tuberculosis

Design outcomes

Primary

MeasureTime frameDescription
Tuberculosis diagnostic algorithm3 yearsDevelopment of an effective diagnostic algorithm for pediatric tuberculosis after evaluating the following diagnostic tests and sampling methods: * Clinical examination * Chest X-rays * Abdominal ultrasound * IGRAs * Xpert MTB/RIF * Gastric aspirate * String test * Nasopharyngeal aspirate * Stools sample * Sputum samples

Secondary

MeasureTime frameDescription
Evaluation of the QuantiFERON(R)-TB Gold In-Tube6 monthsEvaluation of the sensitivity, specificity, positive and negative predictive values of an in-vitro Interferon Gamma Release (IGRAs) : the QuantiFERON(R)-TB Gold iIn-Tube, for the diagnosis of TB in HIV infected children
Percentage of TB diagnosis sampling procedures actually performed6 monthsTo assess the feasibility of the following TB sampling procedures: * the string test * the nasopharyngeal aspirate * stool sample
Evaluation of the morbidity (IRIS, drug toxicity and other opportunistic infections) and mortality in TB-HIV co-infected childrenat 6 month of TB treatment
Comparison of two in-vitro IGRAs6 monthsComparison of the performances of two in-vitro IGRAs: the QauntiFERON(R)-TB Gold In-Tube and the T.SPOT-TB(R), for the diagnosis of tuberculosis in a sub-group of HIV infected children.
Evaluation of the Xpert MTB/RIF assay6 monthsEvaluate the sensitivity, specificity, positive and negative predictive values of the Xpert MTB/RIF assay
Comparison of the Xpert MTB/RIF test to the gold standard (culture of gastric aspirates or sputum)6 months
Comparison of the performance Xpert MTB/RIF assay on sampling methods other than the reference method (gastric aspirate and sputum)6 monthsEvaluation of the Xpert MTB/RIF assay on the following sampling methods: * String test * Nasopharyngeal aspirates * Stool samples
Specificity and sensibility of TB diagnosis sampling procedures compared to TB diagnosis gold standard (sputum or gastric aspirate culture)6 monthsTo assess the performance of the following TB sampling procedures: * the string test * the nasopharyngeal aspirate * stools sample

Countries

Burkina Faso, Cambodia, Cameroon, Vietnam

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 8, 2026