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Premature Birth clinical trials

View clinical trials related to Premature Birth.

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NCT ID: NCT03990116 Recruiting - Premature Infant Clinical Trials

Efficacy of Lateral Kangaroo Care in Hemodynamic Stabilization of Premature Infant.

Cangulat
Start date: May 10, 2019
Phase: N/A
Study type: Interventional

The objetive of the study is to evaluate the non-inferiority or the equivalence of the kangaroo care position, in lateral versus traditional one in prone measuring the stability of several parameters in premature infants less than 28 weeks of gestational age during the first 5 days of life.

NCT ID: NCT03985462 Withdrawn - Clinical trials for Stem Cell Transplant Complications

Very Small Embryonic-like Stem Cells for Ovary

Start date: July 3, 2019
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this study is the safety and efficacy of autologous very small embryonic-like stem cells(VSELs) to premature ovarian failure.

NCT ID: NCT03979196 Terminated - Preterm Birth Clinical Trials

Inpatient vs Outpatient Management of Short Cervix

Start date: June 6, 2019
Phase: N/A
Study type: Interventional

The presence of short cervix during pregnancy is a risk factor for preterm birth though in many cases women will eventually deliver at term or near term. While there are proven treatments such as cerclage and progesterone that can improve pregnancy outcomes, many women are advised to limit their activity, are put on bed rest, or admitted to hospital for inpatient management. Presently, there is no evidence that hospital admission of women with short cervix is beneficial and prolongs the pregnancy. The investigators propose to examine whether inpatient management results in comparable outcomes to outpatient management for women with short cervix.

NCT ID: NCT03977259 Recruiting - Preterm Birth Clinical Trials

Targeting Human Milk Fortification to Improve Preterm Infant Growth and Brain Development

Start date: January 31, 2020
Phase: N/A
Study type: Interventional

This study is a randomized trial comparing 2 methods of human milk fortification for preterm infants in the neonatal intensive care unit (NICU). All participating infants will receive a human milk diet comprising maternal and/or donor milk plus multi-component and modular fortifiers. In one group (control), the milk will be fortified according to routine standard of care. In the other group (intervention), the fortification will be individually targeted based on the results of point-of-care human milk analysis. Outcomes include physical growth in the NICU and after discharge, brain structure by magnetic resonance imaging at term equivalent age, and neurodevelopment at 2 years.

NCT ID: NCT03976063 Recruiting - Clinical trials for Preterm Premature Rupture of Membrane

Tocolysis in the Management of Preterm Premature Rupture of Membranes Before 34 Weeks of Gestation

TOCOPROM
Start date: October 7, 2019
Phase: Phase 3
Study type: Interventional

The purpose of this study is to assess whether short-term (48 hr) tocolysis reduces perinatal morti-morbidity in cases of PPROM at 22 to 33 completed weeks' gestation.

NCT ID: NCT03975764 Not yet recruiting - Gut Microbiome Clinical Trials

Fecal Microbiota in Preterm Birth

Start date: October 1, 2019
Phase:
Study type: Observational

We will compeer fecal microbiome in preterm birth with fecal microbiome of team labor

NCT ID: NCT03974724 Recruiting - Preterm Birth Clinical Trials

Preterm Birth Prediction by Measurement of Biomarkers in Cervical Vaginal Fluid

PBMBCVF
Start date: May 1, 2019
Phase:
Study type: Observational

The purpose of this study is to determine the predictive value of 7 biomarkers cervical vaginal fluid on future preterm birth in pregnant women whose gestational age are 16 to 24 weeks.

NCT ID: NCT03972761 Not yet recruiting - Clinical trials for Premature Childbirth

Evaluation of Brain Plasticity in Premature Infants at School Age After Cognitive Remediation

EPIREM
Start date: September 27, 2019
Phase: N/A
Study type: Interventional

Infantile brain plasticity is still a poorly known phenomenon. However, neuropsychological disorders and behavioral deficits are common disorders that can have serious consequences for school enrollment, family and social adjustment, as well as repercussions on future adult lives. In addition, generally very premature infants (TGP) have identifiable executive function disorders (EF), particularly those involving attentional processes such as working memory (WM). The main objective of the study is to evaluate the effects of cognitive remediation (CR) strategies on the brain plasticity of the cortical areas involved in the management of WM in school-aged TGP children (8 years). The secondary objective of the study is to evaluate the action of CR on the development of cortical areas concerned It is a monocentric, prospective and comparative study of the exposed type (to cognitive remediation) - unexposed. Recruitment and data collection are carried out prospectively, in connection with the original study (EPIREMED). Included patients will be explored by Magnetic Resonance Imaging (MRI) 3 resting state Tesla. The main hypothesis is that CR strategies have a beneficial effect on the cognitive processing of visual-spatial executive functions, but also on the cortical areas involved in brain plasticity in general (indirect benefits); not to mention the psychological benefits ad hoc to such studies (self-esteem, increased concentration, new stress management strategies put in place). The ultimate objective of this study is to better understand the mechanisms of cerebral plasticity concerning higher executive functions. Moreover, this study should make it possible to confirm the improvement of the overall fate of the child by better understanding the neuropsychological and anatomical origins of his disorders. Interventions taking into account the environment of the very premature baby are necessary because it is closely linked to the developmental future.

NCT ID: NCT03963011 Terminated - Premature Infant Clinical Trials

NEC Screening Abdominal Radiograph vs Bowel Ultrasound in Preemies

Start date: December 20, 2018
Phase: N/A
Study type: Interventional

The overall primary objective is to establish the feasibility and pilot the design and delivery of a diagnostic randomized controlled trial (RCT) of BUS (bowel ultrasound) for NEC evaluation which will lead to a successful application for a larger, multi-center clinical trial in the future. This program of research is anticipated to have a significant positive impact in the timely and accurate diagnosis of NEC in preterm infants.

NCT ID: NCT03961139 Recruiting - Clinical trials for Bronchopulmonary Dysplasia

Continuous Versus Intermittent Bolus Feeding in Very Preterm Infants - Effect on Respiratory Morbidity

CONFER
Start date: December 3, 2019
Phase: N/A
Study type: Interventional

Chronic Lung Disease (CLD) of Prematurity is a common yet challenging co-morbidity affecting extremely premature newborns. Multifactorial influences leading to this co-morbidity is known and targeted in various research studies. Gastroesophageal reflux (GER) is common among the same cohort of patients. The investigators hypothesize that recurrent milk reflux into the airways of the premature babies worsen the inflammation of premature lungs and is a major contributor of CLD. The investigators hypothesize that Continuous feeding (CF) minimises GER and micro-aspiration, thereby reducing the incidence and severity of CLD in high-risk infants. Our aim is to compare the effect of intermittent bolus versus continuous intra-gastric feeding on the incidence and severity of CLD in very low birth weight infants ≤ 1250 grams.