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Pediatrics clinical trials

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NCT ID: NCT01460329 Completed - Critical Illness Clinical Trials

Comparing Cardiac Output Measurements in Critically Ill Children Using USCOM and Transthoracic ECHO

Start date: October 2011
Phase: N/A
Study type: Observational

The purpose of this study is to compare the accuracy and precision of two non-invasive methods of measuring cardiac output in critically ill children (<18 yrs). The participants will include any patient admitted to Pediatric intensive care unit (PICU) requiring a trans-thoracic ECHO (TTE) as part of their treatment plan. Measurements of intermittent cardiac output will be obtained and compared on participants using standard 2-D TTE and Ultrasound Cardiac Output Monitor (USCOM).

NCT ID: NCT01418846 Completed - Pediatrics Clinical Trials

Determination of Voriconazole Levels in Saliva - Validation in Specific Subsets of Patients

Start date: October 2012
Phase: N/A
Study type: Observational

The purpose of this study is to investigate the intra-saliva penetration of voriconazole in different subpopulations. The goal is to develop, optimize and validate an easy, non-invasive and painless procedure for Therapeutic Drud Monitoring of voriconazole that can be used in children, ambulatory patients and in patients in whom blood drawing is difficult.

NCT ID: NCT01344512 Completed - Pediatrics Clinical Trials

Population Pharmacokinetics of Anti-infectious Drugs in Children

PHARMA-A
Start date: June 2011
Phase: N/A
Study type: Interventional

The Pharm A project is a French national collaborative project aiming to determine the population pharmacokinetics of ceftazidime, ciprofloxacin, and voriconazole in paediatric patients aged one month to five years.

NCT ID: NCT01331811 Completed - HIV Clinical Trials

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

Start date: April 2011
Phase: N/A
Study type: Interventional

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

NCT ID: NCT01145859 Completed - Venous Thrombosis Clinical Trials

Rivaroxaban Pharmacokinetics/Pharmacodynamics (PK/PD) Study in Pediatric Subjects

Start date: November 2010
Phase: Phase 1
Study type: Interventional

The first study with rivaroxaban in pediatric subjects is a Phase I study, where the pharmacokinetic/pharmacodynamic (PK/PD) profile of rivaroxaban will be investigated to confirm that the exposure is comparable to adults. This study is a single dose study with multiple PK/PD measurements in pediatric subjects at the end of their Venous Thromboembolism (VTE) treatment.

NCT ID: NCT01140386 Completed - Clinical trials for Venous Thromboembolism

Prevalence and Risk Factors of Venous Thromboembolism in Hospitalized Pediatric Patients

pediatric DVT
Start date: May 2009
Phase: N/A
Study type: Observational

The issue to be studied is the prevalence of venous thromboembolism (VTE) in hospitalized pediatric patients, and to identify if there are subgroups of patients who may be at higher risk. There are two hypotheses that will be looked at in this study. The first hypothesis is that individual risk factors for VTE in hospitalized pediatric patients are: age >14, obesity, black race, female sex, presence of a central venous line (CVL), traumatic mechanism of injury, orthopaedic surgery, and use of oral contraceptives. The second hypothesis is that risk factors have an additive effect such that risk stratification can be developed to identify those patients with the highest risk.

NCT ID: NCT01139294 Completed - Dehydration Clinical Trials

Descriptive Study of Cardiac Output During Rehydration With Recombinant Human Hyaluronidase in Pediatrics

Hylenex
Start date: February 2010
Phase: Phase 4
Study type: Interventional

The purpose of this study is to non-invasively study the reflective changes in cardiac output as response to fluid therapy in the pediatric moderate hypovolemia/dehydrated pediatric patients using sub-q rehydration using Hylenex augmented subcutaneous infusion of fluids and electrolytes compared to intravenous methods.

NCT ID: NCT01043562 Completed - Pediatrics Clinical Trials

Precise Measurement of Pediatric Defibrillation Thresholds

Start date: June 4, 2009
Phase: N/A
Study type: Observational

Patients who receive an implantable cardioverter-defibrillator (ICD) usually undergo testing at the end of the ICD procedure to measure the amount of energy able to successfully defibrillate the heart (defibrillation threshold testing, or DFT). This study proposes to perform that measurement in pediatric patients already undergoing clinically necessary ICD procedures, with the measurement performed using a binary search method that has been previously validated in adult cohorts. We hypothesize that pediatric DFTs, when precisely measured, may be lower than previously assumed from extrapolation of adult data.

NCT ID: NCT01022905 Completed - Cancer Clinical Trials

Vaccine Responses to Influenza A H1N1/09 Immunization in High-risk Patients

Start date: November 2009
Phase: Phase 4
Study type: Interventional

The objective of this study is to assess vaccine responses to novel adjuvanted influenza A(H1N1) vaccines in patients at high risks of influenza A(H1N1) complications.

NCT ID: NCT00857727 Completed - Anesthesia Clinical Trials

Use of Dexmedetomidine to Reduce Emergence Delirium Incident in Children

DexPeds
Start date: August 2009
Phase: Phase 3
Study type: Interventional

Emergence delirium (ED) from general anesthesia posts risk and harm to pediatric population undergo general anesthesia. The purpose of the study is to compare the use of dexmedetomidine versus placebo in reducing the incidence and severity of ED in a pediatric neurosurgical population.