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Pediatric ALL clinical trials

View clinical trials related to Pediatric ALL.

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NCT ID: NCT05779332 Completed - Dental Caries Clinical Trials

Prevalence, Etiology and Effects on Oral Health and Life Quality of Molar Incisor Hypomineralization

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

Molar incisor hypomineralization (MIH) can lead to many clinical conditions and affect oral health-related quality of life (OHRQoL).

NCT ID: NCT05757882 Completed - Pediatric ALL Clinical Trials

Reducing Fasting Time in Children for Sedation

Start date: May 25, 2023
Phase: N/A
Study type: Interventional

Patients are asked to be fasted for certain period of time before sedation to reduce the risk of pulmonary aspiration. However, fasting can be harmful, especially in children who has smaller reserves of energy and fluids compared to the adults. Prolonged fasting may increase nausea, vomiting, dehydration, and hypoglycemia. Therefore, it is important to minimize prolonged fasting time in pediatric patients. This study is aimed to investigate the safety of minimal fasting time (2 hours) compared to the standard fasting time (4 hours) with gastric ultrasound.

NCT ID: NCT05731401 Completed - Chronic Pain Clinical Trials

Expressed Beliefs About the Cause of Pain in a Paediatric Population

EBPain
Start date: September 1, 2021
Phase:
Study type: Observational

The aims of this study are to explore what beliefs children and adolescents manifest about the cause of the pain they describe; to compare whether if there are differences between beliefs by age and by persistence of pain; and to relate explanations of the cause of pain with current scientific evidence to determine if these beliefs are erroneous.

NCT ID: NCT05705206 Completed - Pediatric ALL Clinical Trials

Feasibility and Accuracy of Core Temperature Measurements Using the Esophageal Temperature Probe Inserted Through the Gastric Lumen of Supraglottic Airway Device in Pediatrics

Start date: March 25, 2021
Phase:
Study type: Observational [Patient Registry]

In pediatric patients, the accuracy of body temperature measured with an esophageal temperature probe placed through the gastric lumen of the supraglottic airway device is investigated.

NCT ID: NCT05665712 Completed - Clinical trials for Congenital Heart Disease

Pediatric Enhanced Recovery After Cardiac Surgery

PERCS
Start date: November 1, 2019
Phase:
Study type: Observational

Identify our institution's current perioperative management strategies for pediatric cardiac surgery patients. Identify predictive factors for receiving perioperative care following P-ERACS strategies. Compare outcomes between P-ERACS and non-P-ERACS patients

NCT ID: NCT05656937 Completed - Pediatric ALL Clinical Trials

Oblique Versus Transverse Orientation Approach for Internal Jugular Venous Cannulation in Pediatrics

Start date: February 1, 2021
Phase: N/A
Study type: Interventional

this study aimed to compare oblique versus transverse orientation approach in jugular venous cannulation in term of cannulation success in pediatric heart surgery patients

NCT ID: NCT05642117 Completed - Emergencies Clinical Trials

Pediatric Telephone Center Board 15

CTPC15
Start date: May 1, 2021
Phase:
Study type: Observational

This study evaluates the follow-up of advices given in a Urgent Medical Aid Service (SAMU 29) for every pediatric's emergency call under 15yo and try to evaluate the adhesion's factors.

NCT ID: NCT05607355 Completed - Pediatric ALL Clinical Trials

Measurement of Spinal Mobilization in Pediatric Population

Start date: November 1, 2022
Phase:
Study type: Observational

The goal of this cross-sectional study is to measure the biomechanical parameters during a vertebral mobilization delivered by chiropractors on patients of five years old of age and younger. The main questions it aims to answer are: - What is the force and rate of force application of spinal mobilizations in children consulting in chiropractic? - What are the adverse events observed by legal tutors immediately following the intervention received by the child? Participants will receive the clinically indicated spinal mobilization by their treating chiropractor. The chiropractor will have a small sensor on the finger during the delivery of the spinal mobilization. The legal tutor will complete a questionnaire immediately after the intervention to report adverse events.

NCT ID: NCT05565040 Completed - Surgery Clinical Trials

Concealed Penis in Pediatric Age Group

Start date: June 1, 2018
Phase: N/A
Study type: Interventional

Background: Comparison between three different surgical techniques in the management of concealed penis. Methods: This prospective interventional non-randomized study included 150 pediatric patients with concealed penis. They were distributed equally into three groups; group A; patients treated by phallopexy only, group B; patients treated by complete dissection and excision of dartos fascia & group C; patients treated by both phallopexy and dartos excision.

NCT ID: NCT05498402 Completed - Cardiac Arrest Clinical Trials

Effect of IAM With an I-gel® on Ventilation Parameters in Simulated Pediatric OHCA

Start date: January 30, 2023
Phase: N/A
Study type: Interventional

Pediatric cardiac arrest occurs most in the prehospital setting. Most of them are due to respiratory failure (e.g., trauma, drowning, respiratory distress), where hypoxia leads to cardiac arrest. Generally, emergency medical services (EMS) first use basic airway management techniques i.e., the use of a bag-valve-mask (BVM) device, to restore oxygenation in pediatric OHCA victims. However, these devices present many drawbacks and limitations. Intermediate airway management, i.e., the use of SGA devices, especially the i-gel® has several advantages. It has been shown to enhance both circulatory and ventilatory parameters. There is increasing evidence that IAM devices can safely be used in children. In two pediatric studies of OHCA, American paramedics had significantly higher success rates with SGA devices than with TI. A neonatal animal model showed that the use of SGA was feasible and non-inferior to TI in this population. However, data regarding the effect of IAM with an i-gel® versus the use of a BVM on ventilation parameters during pediatric OHCA is missing. The hypothesis underlying this study is that, in case of pediatric OHCA, early insertion of an i-gel® device without prior BVM ventilation should improve ventilation parameters in comparison with the standard approach consisting in BVM ventilations.