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Pediatric ALL clinical trials

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NCT ID: NCT03385681 Completed - Postoperative Pain Clinical Trials

Pediatric Pain Management - an Intervention Study

Start date: September 2014
Phase: N/A
Study type: Interventional

This study will explore nurses' pediatric postoperative pain management knowledge and clinical practices. The aim is to evaluate if a tailored educational intervention will improve nurses' knowledge and attitudes of pain management and pain management practices. The intervention offered is education and skills training. The study has a pre-post design and a comparison group. Data is collected before the intervention is started (baseline T1) and again one month (T2) and six months (T3) after the intervention. Nurses working in six postoperative units are participating. The units are the largest pediatric postoperative units of each of the six university hospitals covering all health regions in Norway. Three different approaches will be used to collect data (survey with questionnaire, observations of clinical practice, and interviews with children).

NCT ID: NCT03378830 Completed - Sleep Apnea Clinical Trials

Pain at Home After Tonsillectomy With or Without Adenoidectomy

Start date: December 19, 2017
Phase:
Study type: Observational

The study type is a prospective observational cohort study of children undergoing adenotonsillectomy (T&A). The study will recruit the annual caseload of children undergoing T&A at the Montreal Children's Hospital, QC, Canada; aiming for 200 children. There are no interventions. The purpose of this study is to determine the severity and duration of postoperative pain after T&A and to link the severity of this pain with the severity of sleep disordered breathing.

NCT ID: NCT03372642 Completed - Pediatric ALL Clinical Trials

Effectiveness of Subtalar Arthroereisis With Endorthesis for Pediatric Flexible Flat Foot

Start date: March 1, 2016
Phase: N/A
Study type: Observational

Pediatric flexible flatfoot is sometimes asymptomatic but it can also cause physical impairment, pain, and difficulty walking. We evaluate the radiographic effectiveness of intervention of subtalar arthroereisis with endorthesis for pediatric flexible flatfoot with final follow-up at skeletal maturity.

NCT ID: NCT03369847 Completed - Asthma Clinical Trials

Inhaled Steroids for Pediatric Asthma at Pediatric Emergency Medicine Discharge

Start date: September 10, 2017
Phase: Phase 4
Study type: Interventional

This study evaluates the initiation of inhaled corticosteroids upon discharge from the pediatric emergency room in children under 18 presenting with asthma exacerbation. Half of the patients will receive a prescription for inhaled corticosteroids in addition to standard care, and half of the patients will receive standard card alone.

NCT ID: NCT03359421 Completed - Trauma Clinical Trials

Trauma Routing Algorithm for Pediatrics

TRAP
Start date: November 27, 2017
Phase:
Study type: Observational [Patient Registry]

Traumatic injury is the leading cause of pediatric death in the United States for those forty-four years of age and younger. Pediatric trauma patients generally have reduced mortality when treated at pediatric trauma centers rather than at adult centers or non-tertiary care facilities. However, nearly half the US pediatric population lives over fifty miles from a Level I or II Trauma Center. While air ambulances are readily available in many jurisdictions, few guidelines and little evidence dictate their appropriate use, especially with regard to pediatric trauma. Previous research is mixed regarding mortality benefit from helicopter Emergency Medical Services (EMS) in injured children. Previous attempts to develop appropriate field triage criteria have failed due to poor sensitivity and specificity for identifying the critically injured child. The current high rate of overtriage is particularly concerning in today's cost-conscious medical community. This research study aims to categorize pre-hospital pediatric trauma in North Carolina, to determine what benefits helicopter EMS provides in the North Carolina trauma system, and to formulate an enhanced screening tool for pre-hospital use to help determine which patients are suitable candidates for helicopter EMS transport.

NCT ID: NCT03356262 Active, not recruiting - Clinical trials for Diabetes Mellitus, Type 2

The QUebec Adipose and Lifestyle InvesTigation in Youth (QUALITY) Cohort

QUALITY
Start date: July 25, 2005
Phase:
Study type: Observational

The QUebec Adipose and Lifestyle InvesTigation in Youth (QUALITY) Cohort study is a unique and comprehensive longitudinal study of 630 Caucasian children and their parents that was designed to investigate the natural history and determinants of childhood obesity and its cardiometabolic consequences.

NCT ID: NCT03318393 Completed - Pediatric ALL Clinical Trials

Study Comparing Bivalirudin Versus Heparin in Neonatal and Pediatric ECMO

Start date: March 25, 2018
Phase: Phase 4
Study type: Interventional

The investigators will prospectively enroll 30 neonatal and pediatric ECMO patients at a single pediatric Level 1 trauma center. The patients will be randomized into two arms; one arm will receive unfractionated heparin and the other arm will receive bivalirudin. There will be 15 patients in each arm for a total of 30 patients. Primary aim will be to compare the efficacy of bivalirudin to unfractionated heparin.

NCT ID: NCT03234777 Completed - Pediatric ALL Clinical Trials

Evaluating a Knowledge Translation Tool for Parents

Start date: November 30, 2017
Phase: N/A
Study type: Interventional

Diarrhea and vomiting in children is a common reason to visit the emergency department. There has been a lot of research on how best to treat children with diarrhea and vomiting who visit the emergency department; however, the care children receive varies by healthcare provider and across hospitals. Additionally, there are things parents can do at home to help manage childhood diarrhea and vomiting and potentially avoid a trip to the emergency department. This shows an urgent need for knowledge translation, that is, efforts to align research knowledge and healthcare practice. Actively involving parents in healthcare decisions has the potential to bridge this gap; however, there is little research on the best ways to communicate complex health information to parents of sick kids. In 2013, a national needs assessment was conducted with parents seeking care for their kids in general emergency departments (trekk.ca). This survey showed that 39% of parents looked for information about their child's health prior to coming to the emergency department and that 44% of these parents looked for this information on the internet. This means that the development and evaluation of digital tools to give parents timely and effective child health information has the potential to reduce unnecessary emergency department visits, empower parents in health decision-making, and ultimately improve child health outcomes. In this project, parents will be actively involved in the evaluation of a digital tool, a whiteboard animation video, designed to communicate the best research evidence on the treatment and management of vomiting and diarrhea in children. In this pilot trial, parents in two emergency departments will be randomized to view the video or a sham video, and then provide quantitative and qualitative data on the potential effectiveness of the video, the perceived benefit and value of the knowledge translation intervention for pediatric vomiting and diarrhea, the feasibility of using iPads and an electronic data collection platform to conduct research with this population, the time required to complete data collection, and parents' willingness to participate in future, similar research.

NCT ID: NCT03192683 Completed - Pediatric ALL Clinical Trials

Modified "Providence" Pedi Cast-Sling vs.Cast and Sling

Start date: April 1, 2016
Phase: N/A
Study type: Interventional

Examining custom made sling vs. off the shelf sling for immobilization following pediatric upper extremity fractures.

NCT ID: NCT03043430 Terminated - Anxiety Clinical Trials

Intranasal Ketamine for Anxiolysis in Pediatric Emergency Department Patients

Start date: May 2016
Phase: Phase 4
Study type: Interventional

Investigators plan to conduct a randomized, double-blinded, controlled study among pediatric patients requiring minor procedures in the Emergency Department setting. Patients will be randomized to one of two arms of intranasal treatments: ketamine 1.0 mg/kg (K) or midazolam 0.3 mg/kg (M). The primary outcome will be change in anxiety using the Modified Yale Preoperative Anxiety Scale (mYPAS).