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Pediatric ALL clinical trials

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NCT ID: NCT04913038 Recruiting - Pain Clinical Trials

Validation of the ANI in Perpubescent Patients in Pediatric Intensive Care Unit.

ANI-EP
Start date: June 29, 2021
Phase:
Study type: Observational

The ANI monitor is a medical device allowing to measure the response of the autonomic nervous system to a painful stimulus. In the pediatric population under general anesthesia, the ANI score can detect failure of locoregional anesthesia; ANI decreases after painful stimulation during surgery, more markedly with smaller doses of Remifentanil. To date, measurement of ANI in sedated children in pediatric intensive care has not been performed or validated as a method of assessing pain and discomfort.

NCT ID: NCT04881240 Recruiting - Pediatric ALL Clinical Trials

Study of CD19-directed Allogeneic Memory T-cell Therapy for Relapsed/Refractory CD19+ Leukemia

Start date: February 14, 2024
Phase: Phase 1
Study type: Interventional

This is a Phase I clinical study evaluating the safety and maximum tolerated dose of a novel CAR T-cell product: allogeneic memory (CD45RA- negative) T-cells expressing a CD19-specific CAR 41BBz (CD19-CAR.CD45RA- negative T-cells) for the treatment of patients ≤ 21 years old with relapsed and/ or refractory CD19-positive leukemia. Primary Objective To determine the maximum tolerated dose (MTD) and characterize the safety profile and dose-limiting toxicities (DLTs) of treatment with allogeneic CD19-CAR.CD45RA-negative T-cells in pediatric, adolescent and young adult patients ≤ 21 years of age, with relapsed and/or refractory CD19-positive leukemia. Secondary Objectives - To evaluate the anti-leukemic activity of allogeneic CD19-CAR.CD45RA-negative T-cells. - To determine rates and severity of graft-versus-host-disease (GVHD) after treatment with allogeneic CD19-CAR.CD45RA-negative T-cells. Exploratory Objectives - To study the expansion, persistence and phenotype of allogeneic CD19-CAR.CD45RA-negative T-cells. - To characterize the cytokine profile in the peripheral blood and CSF after treatment with allogeneic CD19-CAR.CD45RA-negative T-cells. - To assess whether allogeneic CD19-CAR.CD45RA-negative T-cells acquire functional versus exhaustion-associated epigenetic programs. - To determine immune reconstitution post treatment, and the clonal structure and endogenous repertoire of allogeneic CD19-CAR.CD45RA-negative T-cells and relate inferred specificity to CAR response profiles. - To characterize incidence and mechanisms of relapse post-therapy with allogeneic CD19-CAR.CD45RA-negative T-cells.

NCT ID: NCT04731974 Recruiting - Pediatric ALL Clinical Trials

Acute Concussion and Melatonin

Start date: March 1, 2023
Phase: Phase 2
Study type: Interventional

In this study, the investigator plans a randomized trial of melatonin versus placebo post acute pediatric concussion. The investigator hypothesizes that patients with acute concussions managed with melatonin will have improved sleep, decreased depressive symptoms, decreased risk of prolonged concussion symptoms and faster resolution of concussion symptoms.

NCT ID: NCT04675918 Recruiting - Cardiac Arrest Clinical Trials

Pediatric In-Hospital Cardiac Arrest International Registry (PACHIN)

PACHIN
Start date: February 1, 2021
Phase:
Study type: Observational [Patient Registry]

: An intrahospital CA data recording protocol has been designed following the Utstein model. Database is hosted according to European legislation regarding patient data protection. It is drafted in English and Spanish. Invitation to participate has been sent to Spanish, European and Latinamerican hospitals. Variables included, asses hospital characteristics, the resuscitation team, patient's demographics and background, CPR, post-resuscitation care, mortality, survival and long-term evolution. Survival at hospital discharge will be evaluated as a primary outcome and survival with good neurological status as a secondary outcome, analyzing the different factors involved in them

NCT ID: NCT04575883 Recruiting - Clinical trials for Congenital Heart Disease

HIIT in Youth With Congenital Heart Disease (MedBIKE)

Start date: November 22, 2022
Phase: N/A
Study type: Interventional

Congenital heart disease (CHD), the most common birth defect, is present in nearly 1% of the population. CHD patients are associated with intense resource utilization and premature death in adulthood. The risk of premature death is linked with reduced exercise capacity, a finding consistently noted in youth with CHD. Reduced exercise capacity in this population has also been associated with reduce physical activity and health-related quality of life. Cardiac rehabilitation (CR) in adults with acquired heart disease is an established secondary prevention strategy that improves exercise capacity. The investigators propose a prospective clinical trial of a home-based high intensity interval training (HIIT) program using a novel telemedicine-equipped video game-linked cycle ergometer (MedBIKE™) for 10 to 18 year olds with repaired moderate-complex CHD. The pilot study with the MedBIKE has shown promising results. The investigators now seek to study the efficacy of this program in a broader CHD population.

NCT ID: NCT04544878 Recruiting - Covid19 Clinical Trials

Pediatric Intensive Care and COVID-19

CLOVIS
Start date: March 26, 2020
Phase:
Study type: Observational [Patient Registry]

In this prospective longitudinal cohort the investigators reported the clinical, and biological characteristics of all critically ill patients admitted in the pediatric intensive care unit (PICU) of Bicêtre Hospital during the 2019 coronavirus disease (COVID-19) pandemics. Patients were older than 37 weeks of gestational age. No upper limit was set as the unit was transiently converted into a pediatric "adult COVID-19" intensive care unit.

NCT ID: NCT04519632 Recruiting - Pediatric ALL Clinical Trials

Paediatric Palliative Care Pain Management in the Community

PARAMOUNT
Start date: July 15, 2019
Phase:
Study type: Observational

To describe the the barriers and facilitators experienced by carers and healthcare professionals when managing medicines for pain relief for infants, children, and young people approaching the end of life in out of hospital settings.

NCT ID: NCT04477967 Recruiting - Liver Diseases Clinical Trials

Design and Implementation of the Pediatric Liver Transplantation Biobank

Start date: October 1, 2018
Phase:
Study type: Observational [Patient Registry]

The purpose of the pediatric liver transplant biobank is to systematically collect clinical specimens from pediatric end-stage liver disease. It is expected to contribute to the research and development of paediatric end-stage liver disease in the future.

NCT ID: NCT04424095 Recruiting - Pediatric ALL Clinical Trials

Venous Disease in Pediatric Population

VEDIPEDI
Start date: February 1, 2020
Phase:
Study type: Observational

Chronic venous disease (CVD) is widespread in adult subjects of western countries and is responsible of important morbidity and healthcare costs. CVD has never been extensively studied in pediatric population where the early pathophysiological alterations may occur undetected. The aim of this study is to assess the prevalence of CVD searching also for the early clinical and instrumental signs of this disease.

NCT ID: NCT04321200 Recruiting - Pediatric ALL Clinical Trials

PANDA Gym: Automated Assessment of Neurodevelopment in Infants at Risk for Motor Disability

Start date: November 1, 2020
Phase:
Study type: Observational

Early childhood detection of motor delays or impairments provides the opportunity for early treatment which improves health outcomes. This study will use state of the art sensors combined with machine learning algorithms to develop objective, accurate, easy-to-use tools for the early scoring of deficits and lays the foundation for the early prediction of physical disability.