Clinical Trials Logo

Neonate clinical trials

View clinical trials related to Neonate.

Filter by:

NCT ID: NCT05965830 Recruiting - Ultrasound Clinical Trials

Comparing Electromyography of the Diaphragm With Ultrasound in Neonates and Children With Respiratory Support

PROCEDURES
Start date: November 25, 2023
Phase:
Study type: Observational [Patient Registry]

Background of the study: Increased work of breathing, potentially leading to respiratory insufficiency, resulting in the need of (non-) invasive respiratory support is the most common observed problem in the neonatal - and pediatric intensive care unit (NICU/PICU). The diaphragm is the main respiratory muscle. Currently there is not an established technique accessible to observe the (clinical) function of the diaphragm and its role in respiratory insufficiency. New non-invasive modalities are promising, such as transcutaneous diaphragm electromyography (dEMG) and diaphragm ultrasound (dUS). Objective of the study: Our objective is to assess the association between transcutaneous diaphragm electromyography (dEMG) and diaphragm ultrasound (dUS) in the PICU population. Study design: Single center pilot study Study population: The study population consists of children between 0-12 months, admitted to the PICU of the Leiden University Medical Center, with invasive respiratory support. Primary study parameters/outcome of the study: Primary endpoint is to evaluate the association between dEMG and dUS measurements in the PICU population.

NCT ID: NCT05934682 Not yet recruiting - Anesthesia Clinical Trials

Latin American Surgical Outcomes Study in Pediatric Patients

LASOS-Peds
Start date: December 20, 2023
Phase:
Study type: Observational

This prospective, international, multicenter observational study will include hospitals performing pediatric surgery in participating Latin American countries. We aim to assess the incidence of hospital postoperative complications in pediatric surgical patients < 18-years-old in Latin America. We will recruit all consecutive pediatric patients under the age of 18 years who were admitted to participating hospitals undergoing elective and nonelective surgery. The primary outcome is in-hospital postoperative complications up to 30 days after surgery.

NCT ID: NCT05835817 Recruiting - Premature Clinical Trials

Magnetoencephalography by Optical Pumping Magnetometer

MEG OPM
Start date: May 2023
Phase: N/A
Study type: Interventional

MagnetoEncephaloGraphy (MEG) is a method of recording brain activity with high temporal resolution and good spatial resolution, compared to current recording techniques such as ElectroEncephaloGraphy (EEG). The main limitation of MEG is its cost due to the sensors used, the Super Quantum Interference Devices (SQUID). These require a complex infrastructure from an instrumentation point of view to operate, requiring liquid helium, most often at a loss, at increasing cost. Optical Pumping Magnetometers (OPM) type sensors represent a promising alternative to SQUIDs sensors, especially since they do not require helium cooling. The purpose of this project is to Identify biomarkers in Magnetoencephalography of normal brain development in healthy adults, premature and term newborns from "a priori" obtained by the classical technique of High Resolution EEG performed.

NCT ID: NCT05601375 Recruiting - Clinical trials for Fetal Growth Restriction

Speckle Tracking Echocardiography in Infants, Prenatally and Postnatally

STIPP
Start date: September 12, 2022
Phase:
Study type: Observational [Patient Registry]

Comparison of prenatal and postnatal cardiac function assessed by echocardiography using pulsed wave Doppler, Tissue Doppler and speckle tracking (strain and strain rate) between foetuses/neonates with a structural heart disease, with an fetal growth restriction (FGR) and healthy fetuses/neonates.

NCT ID: NCT05296668 Completed - Neonate Clinical Trials

Cuffed Versus Uncuffed Tracheal Tubes in Neonates Undergoing Elective Surgery

Start date: March 1, 2022
Phase: N/A
Study type: Interventional

This thesis aims to assess the safety and efficacy of usage of cuffed ETT in neonate undergoing elective surgeries.

NCT ID: NCT05197868 Completed - Intubation Clinical Trials

Applied Forces During Neonatal Intubation

Start date: January 20, 2022
Phase: N/A
Study type: Interventional

This study will be to compare the forces applied to mannequin airways (at epiglottis and at palate) during direct laryngoscopy and indirect video laryngoscopy with two kinds of blades (straight blade and hyper-angulated blade)

NCT ID: NCT05181423 Recruiting - Biomarkers Clinical Trials

Identification of Noninvasive Biomarkers for Neonates Undergoing Abdominal Surgery

Start date: January 1, 2021
Phase:
Study type: Observational

To identify the potential serum and radiological biomarkers with regard to neonates undergoing abdominal surgery, and to further evaluate the prognostic value of these markers.

NCT ID: NCT05104255 Completed - Neonate Clinical Trials

Neonatal Outcomes in Twin Pregnancies

Start date: January 1, 2017
Phase:
Study type: Observational

Multiple pregnancies are associated with increased maternal and fetal risks compared to singleton pregnancies. Additionally, the cesarean section rate is quite high in multiple pregnancies. This study aimed to evaluate maternal and fetal characteristics and factors affecting fetal outcomes in twin pregnancies delivered by cesarean section.

NCT ID: NCT05085080 Withdrawn - Neonate Clinical Trials

Chinese Neonatal Extracorporeal Life Support Registry (Chi-NELS)

Start date: January 1, 2024
Phase:
Study type: Observational [Patient Registry]

Extracorporeal life support (ECLS), also known as extracorporeal membrane oxygenation (ECMO), is an extracorporeal technique which provides respiratory and cardiac support to patients with respiratory and/or heart failure. Neonates account for a significant proportion of patients requiring ECLS support. While with unique pathophysiology among newborn infants, neonatal ECLS treatment faces different challenges (such as specific indications, anticoagulation, hemodynamic management, high incidences of complications, ect.) from those of elder children or adults. Though neonatal ECMO has been used in developed countries since 1970s, the introduction of neonatal ECMO in China was not reported until 2010s. While on the other hand, there has been a rapid increase of neonatal ECLS cases and centers in China in the past decade with a huge variation of numbers of cases and quality among different centers. Therefore, there is an urgent need to monitor the use and quality of neonatal ECLS in China. The goal of the Chinese Neonatal Extracorporeal Life Support Registry (Chi-NELS) is to maintain a registry of use of ECLS in active neonatal ECLS centers across China, to support quality improvement of neonatal ELCS, clinical research and regulatory agencies.

NCT ID: NCT05075486 Withdrawn - Mortality Clinical Trials

Quality Improvement to Reduce Mortality or Severe Intracranial Hemorrhage in Neonatal Extracorporeal Life Support

Start date: January 1, 2024
Phase: N/A
Study type: Interventional

This is a three-year pre- and post- interventional study to assess the effectiveness of collaborative quality improvement interventions on reducing mortality and severe intracranial hemorrhage (ICH) for neonates receiving extracorporeal life support (ECLS) in China.