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Morbidity;Newborn clinical trials

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NCT ID: NCT06087224 Recruiting - Morbidity;Newborn Clinical Trials

The TELENEO Trial: A Multicenter Trial of Telemedicine for Advanced Neonatal Resuscitations in Community Hospitals

Start date: March 5, 2024
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the impact of real-time audio-video telemedicine consults with a neonatologist (termed teleneonatology) on the early health outcomes of at-risk neonates delivered in community hospitals.

NCT ID: NCT05517577 Recruiting - Clinical trials for Knowledge, Attitudes, Practice

An Integrated Community-based Intervention Package in Improving Maternal and Neonatal Health Outcomes

ICBIP-MNH)
Start date: August 20, 2022
Phase: N/A
Study type: Interventional

This study aims to improve maternal, neonatal and infant health outcomes through an integrated community-based intervention package in Jimma Zone, Southwest Ethiopia.

NCT ID: NCT05397678 Recruiting - Morbidity;Newborn Clinical Trials

Trial to Compare BCG-Bulgaria and BCG-Denmark

BCGSTRAIN IV
Start date: October 21, 2022
Phase: Phase 4
Study type: Interventional

The trial will be a two-year outcome assessor-blinded RCT at the maternity ward of Hospital Simão Mendes (HNSM) in urban Bissau, Guinea-Bissau to compare vaccination with Bacillus Calmette-Guérin (BCG) Danish strain (AJ Vaccines, Copenhagen 1331 strain) versus BCG-Bulgaria (BB-NCIPD, BCG-SL 222 Sofia strain) 1:1 in 15,000 infants with respect to mortality, morbidity and case-fatality rate during hospital admission. The trial will also examine the association between BCG strains and BCG skin reaction kinetics and characteristics. As a secondary aim, this large study will be used to further evaluate the role of maternal BCG immune priming for overall health, since there are indications that the maternal BCG scar status influences offspring health outcomes.

NCT ID: NCT05381285 Not yet recruiting - Mortality Clinical Trials

Survival Model for Preterm Infants

Start date: June 1, 2024
Phase:
Study type: Observational

Study Title Predictive Model of Mortality and Major Morbidity in Preterm Neonates in the Perinatal Period Internal ref. no. / short title Survival Model Study Design Observational Population-based Cohort Study Planned Sample Size Retrospective analysis of Database Planned Study Duration 6-months Primary Objectives To derive a mathematical model for predicting mortality and the composite of mortality/major-morbidity before and immediately after birth in preterm infants Secondary Objectives Statistical Methodology and Analysis Mixed-model multivariable logistic regression analysis

NCT ID: NCT05116670 Completed - Morality Clinical Trials

Comparison of Care Practices, Mortality and Morbidity of Very Preterm Infants Between Two Tertiary Centers in Northwest and South of China

Start date: October 15, 2021
Phase:
Study type: Observational

Care practices, mortality and morbidity of very premature infants from two different tertiary centers were collected and compared, in order to discover areas for improvement where these two newborn centers can learn from each other.

NCT ID: NCT04531839 Withdrawn - Morality Clinical Trials

Improving Outcome of Very Preterm Infants Using Collaborative Quality Improvement

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

A multicenter interventional study using evidence-based collaborative quality improvement to reduce mortality and major morbidities of very preterm infants in six neonatal centers in Shanghai

NCT ID: NCT04214795 Active, not recruiting - Morbidity;Newborn Clinical Trials

Antenatal Steroids Effect on Mortality and Respiratory Outcomes in Preterm Infants

Start date: January 1, 2012
Phase:
Study type: Observational [Patient Registry]

The aim is to evaluate the impact of a complete course of antenatal steroids treatment on mortality and main morbidities in a current population of preterm infants.

NCT ID: NCT04145713 Not yet recruiting - Asphyxia Neonatorum Clinical Trials

Effects of Probiotic Mixture Supplementation and Evaluation of Intestinal Mucosal Tolerance and Gut Microbiome in Newborns With Perinatal Asphyxia Receiving Hypothermic Treatment

VISNAT
Start date: January 1, 2020
Phase: Phase 3
Study type: Interventional

The VISNAT trial is a PILOT STUDY due to absence of previous evidences in literature on using probiotic in newborns with perinatal asphyxia. It is designed as a randomized, placebo-controlled, blinded, multicentre superiority trial with two parallel groups and a primary outcome of mortality and/or disability at 18 months of age. After informed consent is obtained from both parents, randomization will be performed as block randomization with a 1:1 allocation using a computer-generated allocation sequence, while the allocation concealment will be performed using locked bags. Randomization data and allocation list will be stored in a secure place and will not be available to any of the components of the study apart of data collectors. Participant files will be stored for a period of 10 years after completion of the study. All the components of the study will be blinded including: participants and their parents, healthcare providers, outcome assessors, data collectors, data analysts.

NCT ID: NCT04103489 Completed - Preeclampsia Severe Clinical Trials

The Use of Eculizumab in HELLP Syndrome

Start date: February 23, 2021
Phase: Phase 1
Study type: Interventional

This research study is being performed to see if women diagnosed with early preterm Hemolysis, Elevated Liver Enzymes, Low Platelets (HELLP) syndrome (estimated gestational ages of 23-30 weeks) benefit from a medication called eculizumab (ECU). This drug blocks a part of the immune system called complement. By blocking this part of the immune system, eculizumab may stop or reverse the progression of the HELLP syndrome disease. The investigators will also look to see if this drug is effective and benefits both the mother and fetus.

NCT ID: NCT03367013 Active, not recruiting - Preterm Infant Clinical Trials

Lactoferrin Infant Feeding Trial - LIFT_Canada

Start date: February 16, 2018
Phase: Phase 3
Study type: Interventional

This is a multicentre, phase III, 2-arm, masked randomized controlled trial. The primary hypothesis is that oral bovine lactoferrin (bLF), through its antimicrobial, antioxidant and anti-inflammatory properties, will reduce the rate of mortality or major morbidity in very low birth weight (VLBW) preterm infants.