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Premature Birth clinical trials

View clinical trials related to Premature Birth.

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NCT ID: NCT02640703 Completed - Premature Birth Clinical Trials

Effect of Morning vs. Evening Vaccination on Hypoxia and Bradycardia of Preterm Infants: a Randomised Controled Trial

Start date: March 2015
Phase: Phase 3
Study type: Interventional

Hypoxia/bradycardia are common symptoms after vaccination of preterm infants. Adults show diurnal variations in vaccination response, due to circadian regulation of the immune system. The investigators plan to investigate whether preterm infants also show differences in hypoxia/bradycardia rate upon morning vs. evening vaccination. Hypoxia/bradycardia is recorded by pulse oximetry starting 24 hours before until 48 hours after vaccination; parents also kept a sleep-diary. 24 hours after vaccination interleukin-6, interleukin-1β and C-reactive protein get determined. To control vaccination response, pertussis- and haemophilus-titers are determined before vaccination and at 4 months corrected age.

NCT ID: NCT02640664 Completed - Clinical trials for Retinopathy of Prematurity (ROP)

Rainbow Extension Study

RainbowExt
Start date: June 16, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study was to evaluate the long term efficacy and safety of intravitreal ranibizumab compared with laser ablation therapy in patients who were treated for retinopathy of prematurity (ROP) in the core study CRFB002H2301 (NCT02375971)

NCT ID: NCT02640638 Completed - Pregnancy Clinical Trials

A RCT of CenteringPregnancy on Birth Outcomes

CRADLE
Start date: February 24, 2016
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate whether CenteringPregnancy group prenatal care can improve preterm birth rate and other birth outcomes, maternal psychosocial and behavioral outcomes, and decrease the racial difference in selected birth outcomes among African American and White women, compared to individual prenatal care.

NCT ID: NCT02632266 Completed - Clinical trials for Complication of Prematurity

Effect of Extensively Hydrolyzed Liquid Human Milk Fortifier on Growth and Tolerance in Moderately Premature Infants

Start date: July 2015
Phase: Phase 4
Study type: Interventional

The purpose of this study is for the researchers to examine the safety and efficacy of liquid human milk fortifier (HMF) in moderately preterm infants compared to powdered human milk fortifier.

NCT ID: NCT02630147 Completed - Premature Birth Clinical Trials

Effects of Vanilla on Hypoxic Intermittent Events in Premature Infants

Vanilla
Start date: November 2015
Phase: N/A
Study type: Interventional

The purpose of this study is to evaluate the effect of vanilla odor on hypoxic intermittent events in premature infants born between 32.0 and 33.6 weeks of gestational age.

NCT ID: NCT02628821 Completed - Preterm Infants Clinical Trials

The Effectiveness of Non-Invasive Ventilation Use in Preterm Infants.

Start date: January 2012
Phase:
Study type: Observational

Prospective observational study of SNIPPV use in preterm infants of less than 32weeks of gestation from January 2012 to December 2015. Previous respiratory status is analyzed as well as respiratory outcomes and possible secondary side effects. SNIPPV is used to prevent Intubation in Infants in which nCPAP has already failed (Infants that met intubation criteria) and also is used electively for extubation when nCPAP extubation has previously failed or infants with Prolonged mechanical ventilation (more than 15 days) with high respiratory parameters (PMAP > 10 cmH2O and FiO2>35%).

NCT ID: NCT02626299 Completed - Preterm Birth Clinical Trials

Assessment of DHA On Reducing Early Preterm Birth

ADORE
Start date: June 8, 2016
Phase: Phase 3
Study type: Interventional

The purpose of this study is to determine if giving a larger amount of DHA than currently included in some prenatal supplements can reduce early preterm birth (birth before 34 weeks of pregnancy).

NCT ID: NCT02623881 Completed - Pregnancy Clinical Trials

Cervical Pessary vs. Vaginal Progesterone for Preventing Premature Birth in IVF Twin Pregnancies

Start date: March 4, 2016
Phase: N/A
Study type: Interventional

To compare the effectiveness of cervical pessary (Arabin) and vaginal progesterone for preventing premature birth in twin pregnancies after IVF

NCT ID: NCT02622373 Completed - Preterm Birth Clinical Trials

Impact of Currently Recommended Postnatal Nutrition on Neonatal Body Composition

Start date: June 2015
Phase: N/A
Study type: Observational

The purpose of this study is to gain information that may be useful in helping to figure out better or newer ways to provide nutrition to babies born premature.

NCT ID: NCT02620943 Completed - Anemia Clinical Trials

Dietary Diversity is Associated With Maternal Anemia and Key Prenatal Outcomes in Ethiopia

Start date: August 2014
Phase: N/A
Study type: Observational

Background: Maternal and child under-nutrition is the underlying cause of death for millions across the globe. Anemia during pregnancy is among the leading nutritional disorders with serious short and long term consequences to both the mother and fetus. Objective: Examine the effect of dietary diversity on maternal anemia, nutritional status and key pregnancy outcomes of pregnancy. Methods: A prospective cohort study design, involving a total of 432 eligible pregnant women, in their second antenatal care visit was conducted between August 2014 to March, 2015. The individual dietary diversity Score (IDDS) was used as the exposure variable to select, enroll and follow the mothers. Epi-data, SPSS and STATA software are used to enter and analyze the data. Chi-square test, independent 't'-test, and GLM are used to calculate risk, association and differences between key variables at P < 0.05