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Infant Conditions clinical trials

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NCT ID: NCT06309199 Not yet recruiting - Clinical trials for Functional Gastrointestinal Disorders

Prevalence of FGIDs and Probiotics Study

PROOF
Start date: March 2024
Phase: N/A
Study type: Interventional

This is a study to evaluate the prevalence of FGIDs in infants using the Thai version of Rome IV diagnostic questionnaire for functional gastrointestinal disorders in infants and evaluate the efficacy of Limosilactobacillus reuteri DSM 17938 to prevent FGIDs in infants.

NCT ID: NCT03640715 Not yet recruiting - Infant Conditions Clinical Trials

Validation of a Screening Tool for Social and Health Vulnerability in Pediatric Clinical Practice

ENVU
Start date: October 2018
Phase: N/A
Study type: Interventional

In 2014, the french hospital emphasized the need for tools to screen for social fragility in order to make explicit the choices of orientation of patients. To date, caregivers do not have any tools or clinical benchmarks for individual assessment of pediatric social and health vulnerability. The use of the Health Care Access Permanence Services (PASS) is intended to facilitate access to the health care system for people in precarious situations with care and social support within and outside the institutions. health. The hypothesis tested is that the use of a formalized tool makes it possible to improve the detection of pediatric social vulnerability and to overcome reluctance to practice by a simple, rapid and justified approach with regard to ongoing care. The primary objective is to validate a clinical tool for screening for pediatric social and health vulnerability - Tool: VUlnerable Child (ENVU) -; to allow for an appropriate orientation of the patient care pathway. The metrological validation of diagnostic performances (sensitivity, specificity, positive and negative likelihood ratios) will be studied in confrontation with the opinion of an expert caregiver in the care of vulnerable populations. This multicenter cross-sectional validation study of the screening tool will be conducted in two SAUPs with a pediatric PASS. 1000 children will be included in the centers for a period of 1 year. Following the introduction of the ENVU tool and after an expert interview, three groups of patients will be identified: Group A: no vulnerability according to expert with no indication of any PASS marker care Group B: probable vulnerability according to the expert with indication of at least one PASS marker care Group C: high vulnerability according to the expert with indication of at least two care markers PASS Group B and C patients will be reviewed at 6 months for a second visit to the ENVU tool. The main evaluation criterion will be the concordance between the indication of the use of the PASS by the "expert" PASS nurse (indicator of a significant social and health vulnerability) and the result of the ENVU tool.