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Premature Birth clinical trials

View clinical trials related to Premature Birth.

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NCT ID: NCT03748472 Completed - Respiratory Disease Clinical Trials

The Effect of Feeding Length on the Oxygenation Instability Among Premature Infants

Start date: May 29, 2019
Phase: N/A
Study type: Interventional

SpO2 instability is in the nature of premature infants. Hypoxic episodes occur spontaneously in many of these infants, especially after the first week of life. Different interventions have been shown to influence the incidence of hypoxemic episodes in premature infants. Premature infants are fed via an NG/OG tube. Feeding length might influence the oxygenation instability among premature infants therefore the aim of this study is to evaluate the changes in oxygenation among preterm infants receiving respiratory support when are fed over 30 min vs over 2 hours, as documented by SpO2 histograms.

NCT ID: NCT03744078 Recruiting - Clinical trials for Induction of Labor Affected Fetus / Newborn

A Randomized Trial of Induction Methods in Premature Rupture of Membranes

Start date: April 15, 2018
Phase: N/A
Study type: Interventional

This study evaluates the addition of transcervical Foley catheter balloon and vaginal prostaglandin E2 induction in premature rupture of membranes. Half of participants will be used combine transcervical Foley catheter balloon and vaginal prostaglandin E2, while the other half will be used alone vaginal prostaglandin E2.

NCT ID: NCT03743207 Completed - Prematurity Clinical Trials

Preterm Infants May Better Tolerate Warmer Feeds

Prematurity
Start date: October 1, 2012
Phase: N/A
Study type: Interventional

Feeding intolerance is frequent among preterm infants in neonatal intensive care units (NICUs). Although there are many studies about enteral nutrition strategies and content in preterm infants, no evidence-based standards exist for the optimal milk temperature for preterm infants. Therefore, in this study the investigators aimed to examine the effects of feeding temperature and the possible morbidities.

NCT ID: NCT03739463 Not yet recruiting - PPROM Clinical Trials

Pro-omega-3, Reduction of Inflammation and Modulation of Prematurity

Pro-MEGA
Start date: December 3, 2018
Phase: N/A
Study type: Interventional

The aim of the project is to decrease the inflammatory status of pregnant women with preterm premature rupture of membranes to delay the initiation of labour that would inevitably lead to premature delivery. The main objective is to measure the mean duration between the initiation of the treatment and delivery in the two groups treated either with MAG-DHA or with the placebo.

NCT ID: NCT03738293 Withdrawn - Prematurity Clinical Trials

Continuous Glucose Monitoring of Late Preterm Birth After Corticosteroids

Start date: December 2019
Phase:
Study type: Observational

Women undergoing late preterm birth are at high risk of delivering a newborn with neonatal hypoglycemia. The investigators plan to monitor interstitial glucose levels prior to delivery in these women in order to develop a better understanding of the relationship between maternal hyperglycemia and neonatal hypoglycemia.

NCT ID: NCT03731611 Completed - Preterm Infant Clinical Trials

Impact of Umbilical Cord Milking in Preterm Neonates With Placental Insufficiency

Start date: April 1, 2019
Phase: N/A
Study type: Interventional

To investigate the effect of umbilical cord milking (UCM) on peripheral hematologic parameters including hematopoietic progenitor cells in premature infants ≤ 34 weeks gestational age with placental insufficiency. We hypothesize that UCM would enhance peripheral CD34 concentration, hemoglobin and reduce prematurity complications like NEC and IVH in preterm infant ≤ 34 week gestational age with placental insufficiency.

NCT ID: NCT03731546 Completed - Preterm Infant Clinical Trials

Effect of Delayed Cord Clamping in Preterm Neonates With Placental Insufficiency

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

To investigate the effect of delayed cord clamping (DCC) on hematopoietic progenitor cells (HPCs), hematological parameters including haemoglobin concentration and hematocrit value in premature infants (34 weeks gestational age or less) with placental insufficiency.We hypothesized that preterm infants with placental insufficiency underwent DDC could have better hematologic parameters and hematopoietic progenitor cells compared to immediate cord clamping.

NCT ID: NCT03728764 Completed - Preterm Infant Clinical Trials

Growth and Safety of a Two-stage Feeding System in Preterm Infants

Start date: October 10, 2018
Phase: N/A
Study type: Interventional

This study evaluates the safety and suitability of the two-stage feeding system in preterm infants.

NCT ID: NCT03715530 Terminated - Preterm Birth Clinical Trials

Use of Placental Alpha Microglobulin-1(PAMG-1) to Diagnose Premature Rupture of Membranes in Pregnant Women

PAMG-1
Start date: September 2007
Phase: N/A
Study type: Interventional

The study is to evaluate the accuracy of a test device called "PAMG-1" to see if a pregnant women has ruptured membranes in comparison to standardly used testing methods.

NCT ID: NCT03714633 Active, not recruiting - Extreme Prematurity Clinical Trials

Stockholm Preterm Interaction-Based Intervention

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

Extreme premature Children will at discharge from Karolinska Hospital and Södersjukhuset in Stockholm be asked to participate in a study, examining the effects of a home-visit based post-discharge program aiming at facilitating the interaction between infants and parents, improving the development of the children, and the parental mental health. The study is a randomized controlled Trial (RCT), hence 50% of the participants will be offered treatment as usual (TAU) with addition of an extended follow-up program. The interaction-based program consists of one initial visit at the hospital followed by nine home-visits and two telephone calls during the child's first year of life. The interventionists are skilled Healthcare professionals with several years of experience from caring for premature infants and their parents. All interventionists have successfully completed a one year further education program, delivered one day per week and containing theoretical lectures, practice with actual cases, supervision on the cases, visits to the different parts of the neonatal care chain and discussions with a representative from the premature family association Sweden.