Clinical Trials Logo

Premature Birth clinical trials

View clinical trials related to Premature Birth.

Filter by:

NCT ID: NCT04423016 Completed - Preterm Birth Clinical Trials

Transitional Cerebrovascular Reactivity in Very Preterm Infants

Start date: February 21, 2018
Phase:
Study type: Observational

The transitional period, defined as the first 72 hours after preterm birth, is often characterized by a significant hemodynamic instability and may also be associated with an impairment of cerebral autoregulation, with relevant clinical implications. The moving correlation coefficient between cerebral oxygenation and heart rate, also defined as TOHRx, has been previously proposed as a marker of cerebrovascular reactivity and provides an indirect estimation of cerebral autoregulation in preterm infants. This study aims to evaluate whether different antenatal, perinatal and postnatal factors may influence cerebrovascular reactivity in very preterm infants during the transitional period.

NCT ID: NCT04413019 Completed - Clinical trials for Preterm Premature Rupture of Membrane

Domiciliary Versus Hospital Management of PPROM

PPROM
Start date: April 15, 2019
Phase:
Study type: Observational [Patient Registry]

This study is designed to compare efficacy & safety of planned domiciliary versus hospital care for women with preterm prelabor rupture of the membranes (PPROM) on fetal, neonatal and maternal outcome.

NCT ID: NCT04408807 Completed - Clinical trials for Retinopathy of Prematurity

Stress Induced by Screening for Retinopathy of Prematurity - Should Speculum and Indentation Rather be Avoided

stressROP
Start date: September 3, 2019
Phase: N/A
Study type: Interventional

The purpose is to assess the hypothesis that indirect ophthalmoscopy for retinopathy of prematurity eye examination (ROPEE) screening without the use of a lid speculum and scleral indentation (speculum-free, SpF) is less painful/stressful than funduscopy with speculum (Sp) and scleral indentation.

NCT ID: NCT04404816 Completed - Clinical trials for Respiratory Distress Syndrome

Effects of Non-invasive Ventilation With Helium-oxygen Mixture in Premature Infants With Respiratory Distress Syndrome

Start date: January 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The use of a mixture of helium with oxygen (heliox) as a breathing gas may be beneficial due to its unique physical properties, such as low density and high carbon dioxide (CO2) diffusion coefficient. In previous studies in neonates with respiratory failure, conventional ventilation with heliox was associated with improved oxygenation and selected respiratory parameters. The use of heliox may increase the effectiveness of intermittent nasal positive pressure ventilation (NIPPV), but knowledge about the effects of such therapy on newborns is limited.The use of non- invasive neurally adjusted ventilatory assist (NIV-NAVA) allows synchronization and assessment of electrical activity of the diaphragm (EaDI) during heliox administration in premature babies with respiratory failure.

NCT ID: NCT04400175 Completed - Premature Birth Clinical Trials

Effects of a Valved Feeding System in Late-preterm Newborns: the Safe Oral Feeding Trial

SOFT
Start date: December 1, 2020
Phase: N/A
Study type: Interventional

Comparing with a randomized controlled trial two different feeding systems in two groups of late-preterm newborns for evaluating which is more efficient in promoting the coordination in the process of sucking-swallowing-breathing and better cardiorespiratory stability. The B-ESP group will be fed with a feeding system with a valved ergonomic teat; the B-STD with a standard feeding system.

NCT ID: NCT04391634 Completed - Respiratory Failure Clinical Trials

Cerebral and Circulatory Effects of Neonatal Volume Targeted Ventilation

Start date: August 1, 2017
Phase: N/A
Study type: Interventional

The aim of the study was to assess the effect of volume targeted vs. pressure-controlled mechanical ventilation (MV) on circulatory parameters and cerebral oxygenation in the extremely preterm infants.

NCT ID: NCT04383340 Completed - Premature Birth Clinical Trials

Sensitivity Training for Parents With Premature Infants

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

This study evaluated the effectiveness of a culturally adapted version of the Mother-Infant Transaction Program (MITP) among Chinese mothers with premature infants in public hospitals in Hong Kong.

NCT ID: NCT04382976 Completed - Preterm Infant Clinical Trials

The Incidence and the Risk Factors of Nephrocalcinosis in Very Preterm Infants

Start date: October 1, 2018
Phase:
Study type: Observational

The study aims to assess the incidence and the risk factors of nephrocalcinosis in very preterm infants using patient data collected during hospitalisation at the Neonatology Centre.

NCT ID: NCT04355949 Completed - Clinical trials for Vitamin D, Vitamin B12 and Folic Acid Among Patients With Premature Ejaculation

Assessment of Serum Levels of Vitamin D, Vitamin B12 and Folic Acid Among Patients With Lifelong Premature Ejaculation and Non-responding to Dapoxetine Treatment.

PE
Start date: February 28, 2020
Phase: N/A
Study type: Interventional

Therefore, this study will aim to assess serum levels of vitamin D, vitamin B12 and folic acid among patients with lifelong PE and non-responding to dapoxetine treatment.

NCT ID: NCT04342585 Completed - Preterm Birth Clinical Trials

Comparison Between Vaginal Pessary and Progestogen in Twin Pregnancy With Short Cervical Length

Start date: October 1, 2019
Phase: Phase 3
Study type: Interventional

A randomized clinical trial comparing vaginal progestogen and vaginal pessary as an intervention for twin pregnancies with short cervical length.