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Pediatric ALL clinical trials

View clinical trials related to Pediatric ALL.

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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: NCT05645133 Terminated - Healthy Clinical Trials

QPlus Pediatric Reference Interval

Start date: February 27, 2023
Phase:
Study type: Observational

Evaluation of coagulation results reported by the Qplus Quantra System to determine pediatric reference range intervals.

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: NCT05528939 Recruiting - Pediatric Cancer Clinical Trials

Feasibility/Acceptability of Attentional-Control Training in Survivors

FAACTS
Start date: June 14, 2023
Phase: N/A
Study type: Interventional

This is a multicenter pilot randomized controlled trial, with an active control condition, of the feasibility, acceptability, and preliminary efficacy of EndeavorRx in a cohort of survivors of acute lymphoblastic leukemia or brain tumor ages 8-16 who are > 1 year from the end of therapy.

NCT ID: NCT05509335 Recruiting - Pediatric ALL Clinical Trials

Ultrasound Assessment On Effectiveness of Cricoid Pressure In Paediatric Population

Start date: August 19, 2022
Phase:
Study type: Observational

Cricoid pressure (CP) confers Grade IIA evidence in preventing gastric insufflation during general anaesthesia. However, a retrospective review of computed tomography scans by Dotson et al. shows that 45% oesophagus is eccentric in the paediatric population aged 1 to 8 years old. In adults, the eccentric oesophagus is associated with reduced CP efficacy in occluding oesophagus. To date, no dynamic real-time study has been done to assess the incidence of the eccentric oesophagus in the paediatric population, the efficacy of CP in occluding eccentric oesophagus, and the effect of anaesthesia on oesophageal position. Any patients aged 1 to 8 years old are eligible to participate This study will be conducted in the operation theatre of UMMC. The investigators plan to perform an ultrasound of the neck throughout the phases of anaesthetic induction and determine the oesophagus position and its compressibility with CP application.

NCT ID: NCT05506683 Recruiting - Pediatric ALL Clinical Trials

Improving Nighttime Access to Care and Treatment; Part 2- Ghana

INACT2-G
Start date: November 16, 2022
Phase: N/A
Study type: Interventional

Globally, leading causes of death among children one month to 5 years old are pneumonia, diarrheal disease and malaria which are treatable early in the disease-course with low-cost medications. However, these diseases can progress to emergencies when access to care is delayed. In response, a telemedicine and medication delivery service (TMDS) was designed to improve nighttime access to pediatric care and treatment. Over 9-months, the TMDS will be implemented in a Ghanaian community to evaluate the clinical safety and operational feasibility of implementing the service.

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.