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Pediatric ALL clinical trials

View clinical trials related to Pediatric ALL.

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NCT ID: NCT03040570 Completed - Hypoxia Clinical Trials

Conservative Versus Liberal Oxygenation Targets in Critically Ill Children

Oxy-PICU
Start date: March 4, 2017
Phase: N/A
Study type: Interventional

A feasibility study to determine if it is possible to perform a safe, adequately powered, and affordable multi-centre study in critically ill children comparing current practice of liberal targets for systemic oxygen levels with more conservative targets.

NCT ID: NCT02995525 Completed - Chronic Pain Clinical Trials

Chronic Pain After Scoliosis and Thoracic Surgery in Children

PEDIACHROII
Start date: December 2016
Phase:
Study type: Observational

The aim of this epidemiologic prospective study is to determine the prevalence of CPSP defined as pain occurring 4 months after scoliosis and thoracic surgery and rated > 3 on a 10 point visual analogue scale or FLACC scale, in children aged from 6 to 18 years. The main objective : prevalence of chronic post surgical pain 4 months after scoliosis ant thoracic surgery in children aged 6 to 18 years. The secondary objectives: the intensity of chronic post surgical pain, the prevalence of neuropathic syndrome and the predictive risk factors.

NCT ID: NCT02993978 Completed - Pediatric ALL Clinical Trials

Design and Evaluation of Care Environment and Technology at Pediatric Radiotherapy

DUMBO
Start date: August 2012
Phase: Phase 2
Study type: Observational

The purpose of the study is to evaluate the effect of changes in the care environment in pediatric radiotherapy. The definitions of the changes is a part of the study, and is constructed in collaboration with the institute of design at Umeå University. The implementation is however not part of the study, but done as part of Clinical routine. The study consist of two parts, where the first 1.5 years are a Control phase where the changes are designed and also function as a baseline period. The following 1.5 years are the case period where the Changes that are accepted for Clinical implementation are implemented. The impact of the changes are evaluated using surveys and interviews of both parents and children

NCT ID: NCT02989675 Terminated - Critical Illness Clinical Trials

SugarFACT - Sugar Requirements For African Children Trial

Start date: December 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact of dextrose administration in severely sick children admitted to hospital with low-glycaemia. The problem: Mortality in children remains high in sub-Saharan African hospitals. While antimalarial drugs, antibiotics and other definitive treatments are well understood, the role of emergency care with supportive therapies such as maintaining normal glucose and electrolyte balances, has been given limited attention. Hypoglycaemia is common in children admitted to hospital in low-income settings. The current definition of hypoglycaemia is a blood glucose level of less than 2.5mmol/l. Outcomes for these children are poor, with a mortality rate of up to 42%. An increased mortality has also been reported among acutely ill children with low-glycaemia, defined as a blood glucose level of 2.5-5.0mmol/l. The reason for increased mortality rates is not fully understood. Study objective: To determine the impact on mortality of a raised treatment cut-off level for paediatric hypoglycaemia, from 2.5mmol/l to 5.0mmol/l. Methodology: Severely ill children admitted to two central Malawian hospitals; Queen Elisabeth Central Hospital, Blantyre and Zomba Central Hospital, with low-glycaemia (2.5-5.0mmol/l) will be randomised into intervention or control groups. The intervention group will be treated with an intravenous bolus of 10% dextrose 5ml/kg followed by a dextrose infusion in addition to standard care while the control group will receive standard care only. Children will be followed until discharge from hospital or death. Primary end-point is in-hospital mortality.

NCT ID: NCT02930850 Completed - Healthy Clinical Trials

Spot-Check Noninvasive Hemoglobin (SpHb) Clinical Validation

Start date: September 2016
Phase: N/A
Study type: Interventional

The purpose study is to report on the accuracy of noninvasive hemoglobin (SpHb) as compared to hemoglobin measurements obtained from a laboratory hematology analyzer.

NCT ID: NCT00229671 Completed - Pediatric ALL Clinical Trials

Medication Errors and Adverse Drug Events (ADEs) in Ambulatory Pediatrics

Start date: September 2001
Phase: N/A
Study type: Interventional

The purpose of this study is to determine the rates of medication errors in pediatric outpatients in 6 office practices. Further, we wish to determine the effectiveness of a computerized physician order entry (CPOE) system in reducing errors.