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Child clinical trials

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NCT ID: NCT02333786 Completed - Child Clinical Trials

Ultrasound-guided Arterial Catheterization in Pediatric Patients

Start date: January 2015
Phase: N/A
Study type: Interventional

Investigators designed a prospective randomized controlled study to compare the long-axis/in-plane and short-axis/out-of-plane methods during the ultrasound-guided arterial catheterization in pediatric patients younger than 5 years old.

NCT ID: NCT02318940 Recruiting - Child Clinical Trials

Femoral Central Venous Access Comparison of 2 Methods

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

The purpose of this study is to compare the effectiveness and safety of the installation of femoral central venous catheter (CVC) ultrasound-guided real-time 2D versus the landmark method

NCT ID: NCT02312388 Completed - Surgery Clinical Trials

Comparison of the Central Venous Catheter Insertion Techniques

Start date: July 2013
Phase: N/A
Study type: Interventional

The purpose of this study is to compare the differences in central venous catheter insertion time, success rate, and complication between thin-wall needle technique and catheter-over-the-needle technique for central venous catheterization in children.

NCT ID: NCT02303561 Completed - Obesity Clinical Trials

The Childhood Health and Asthma Management Program

CHAMP
Start date: June 2014
Phase: N/A
Study type: Interventional

Overweight and obese (OV/OB) children with asthma are at-risk for particularly poor health outcomes including poor asthma control, higher risk of asthma-related symptoms, and decreased quality of life. Weight loss reduces asthma symptoms, improves lung function, and increases quality of life among OV/OB adults with asthma. Little research has examined the impact of weight loss on asthma outcomes in OV/OB youth, and there is little research examining weight management interventions in OV/OB children with asthma. Behavioral family-based lifestyle interventions are successful in producing weight loss in children. To our knowledge, however, there has been no systematic effort to examine the impact of these interventions on weight status and asthma outcomes, nor has there been an effort to tailor these programs to the specific needs of OV/OB children with asthma. The aims of this study are to develop and test the Childhood Health and Asthma Management Program (CHAMP), a behavioral family-based lifestyle intervention that is community-based to promote successful weight and asthma management in OV/OB children with asthma. The investigators propose to develop an intervention based on a previously developed behavioral family-based lifestyle intervention that was community-based and produced positive long term weight status changes in OV/OB children and tailor it for OV/OB children with asthma to create CHAMP. CHAMP will include asthma education and targeting unique barriers to weight management in OV/OB children with asthma. A focus group will be conducted with OV/OB children with asthma, ages 6-12, and their parent(s). Then a pilot randomized controlled trial of the CHAMP intervention with 32 OV/OB children with asthma, ages 6-12 years, and their parent(s). Families will be randomly assigned to CHAMP or a health education group. The investigators hypothesize that participants in CHAMP will have more effective weight and asthma management and child asthma outcomes compared to those in the general education group.

NCT ID: NCT02300701 Completed - Atopic Dermatitis Clinical Trials

Role of Anti-IgE in Severe Childhood Eczema

ADAPT
Start date: December 2014
Phase: Phase 4
Study type: Interventional

To evaluate the efficacy of anti-IgE (Omalizumab/Xolair) in children with severe eczema.

NCT ID: NCT02248493 Completed - Pain, Postoperative Clinical Trials

Intravenous Paracetamol for Postoperative Pain

IVPARACET
Start date: November 2012
Phase: Phase 4
Study type: Interventional

The purpose of this study is to define if intravenous paracetamol may improve analgesia and outcome in pediatric surgical patients treated with non-steroidal anti-inflammatory drugs (NSAIDs) postoperatively. Hypothesis: intravenous paracetamol in a dose 60 mg/kg/24 h IV, given in addition to IV ketoprofen (4,5 mg/kg/24h), improves analgesia and physical recovery in children and adolescents following surgery.

NCT ID: NCT02240368 Completed - Anesthesia Clinical Trials

Performance Evaluation of the Depth of Anesthesia Monitors in Pediatric Surgery

Start date: September 2014
Phase:
Study type: Observational

The purpose of this study is to determine how Bispectral index (BIS) and Entropy EEG monitors agree between themselves and with end-tidal concentration of sevoflurane (ETsevo) in relationship with the age in the pediatric surgery setting. Bispectral index (BIS) and Entropy EEG monitors performance and utility is well established in adult general anesthesia. Their utility is yet undefined in the pediatric population as age seems to affect their ability to track the cerebral hypnotic state in children.

NCT ID: NCT02201680 Completed - Child Clinical Trials

Anxiety Level of Child and Parents During Preoperative Anesthesia Evaluation

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

1. Appreciation of preoperative anxiety in children is important for the anesthesiologist. 2. Several factors defined to effect the anxiety levels preoperatively in children such as , age, previous medical encounters , education level and parental anxiety. 3. This information was tested for Turkish children during the preoperative anesthetic evaluation.

NCT ID: NCT02201628 Completed - Child Clinical Trials

Correlation of Nasopharyngeal (NP) and Lower Oesophageal (LO) Temperatures in Ventilated Children

Start date: June 25, 2014
Phase: N/A
Study type: Interventional

Children lose heat under general anaesthesia, thus temperature is routinely monitored during anaesthesia for all but the shortest cases, and active warming can be used to prevent hypothermia and its resulting complications. Temperature can be measured at several sites dependent on the type of surgery and patient factors. Previously a temperature probe has been sited in the lower third of the oesophagus (swallowing tube) but it is difficult to accurately place this without an X-Ray. Consequently it is more common to use a temperature probe placed in the nasopharynx (where the nose and throat meet), when the child is anaesthetised. However the investigators do not know if the temperature in the nasopharynx correlates well with the real core temperature or not.This prospective, unblinded, agreement study will seek to find an agreement of 2 methods to measure temperature in children undergoing general anaesthesia with a breathing tube that has a leak.

NCT ID: NCT02132273 Completed - Child Clinical Trials

Use of an Educational Story to Prepare Children With Developmental Disabilities for Sleep Study

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

The investigators hypothesize that use of an educational story with pictures illustrating overnight sleep study procedure (also called polysomnography or PSG)accompanied by simple narrative will be a cost-effective, readily accepted intervention that will contribute to successful completion of sleep studies among children with disabilities. Children who have been referred for a clinical sleep study at Kennedy Krieger Institute (KKI) will be enrolled and randomized to either recieve usual care (discussion of polysomnography with referring clinicians) or educational story intervention. Both groups of participants will be asked to complete questionnaries before and after the sleep study. Set-up for the sleep study will be videotaped so that behavior of the child can be evaluated. The investigators will evaluate whether successful study completion differs between the two groups.