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Necrotizing Enterocolitis clinical trials

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NCT ID: NCT03302338 Recruiting - Clinical trials for Necrotizing Enterocolitis

Simulated Amniotic Fluid Solution in Neonates Recovering From GIT Surgeries

Start date: July 2015
Phase: Phase 1
Study type: Interventional

Amniotic fluid plays a significant role in fetal gut maturation and development. The human fetus swallows over 200 ml of amniotic fluid per kilogram of weight each day and such swallowing is essential for normal small bowel development.Growth factors found in the amniotic fluid have been shown to promote proliferation of fetal intestinal cells. As feeding intolerance is a common problem among neonates recovering from surgery for congenital bowel abnormalities, the investigators will study the role of enteral administration of simulated amniotic fluid solution in prevention of feeding intolerance and NEC in neonates recovering from GIT surgeries.

NCT ID: NCT03210831 Recruiting - Clinical trials for Necrotizing Enterocolitis

Early Predictors of Necrotizing Enterocolitis in Neonates

Start date: September 6, 2017
Phase:
Study type: Observational

The goal of this project is to identify neonates who are predisposed to Necrotizing Enterocolitis (NEC). the investigators will determine the effectiveness of non-invasive measures as well as biochemical markers to identify neonates early in the disease process. Thus, the investigators aim to identify infants with NEC prior to the onset of symptoms to institute or test treatments in the long term to prevent the progression of the disease in these infants.

NCT ID: NCT02741648 Recruiting - Anemia Clinical Trials

RBC Irradiation, Anemia and Gut Injury

RBC-mNIRS
Start date: July 2016
Phase:
Study type: Observational

The purpose of this trial is to study the effect that anemia and Red Blood Cell (RBC) transfusions have on oxygen levels in the digestive tracts of Extremely Low Birth Weight (ELBW) infants and to look for possible markers in a baby's blood, urine and/or stool that may lead to a better understanding of what makes an ELBW infant at risk for digestive tract problems such as necrotizing enterocolitis.

NCT ID: NCT02733718 Recruiting - Clinical trials for Necrotizing Enterocolitis

The Impact of Different Feeding Strategies During Packed Red Cell Transfusion on Intestinal Oxygenation

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

This study aims to compare the differences between three different feeding regimens on intestinal oxygenation during packed red blood cell (PRBC) transfusion in premature babies.

NCT ID: NCT02552706 Recruiting - Death Clinical Trials

The Efficacy and Mechanisms of Oral Probiotics in Preventing Necrotizing Enterocolitis

Start date: September 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to investigate the efficacy and its mechanisms of oral mixture probiotics in preventing necrotizing enterocolitis among the preterm very low birth weight infants.

NCT ID: NCT02405637 Recruiting - Clinical trials for Necrotizing Enterocolitis

Simulated Amniotic Fluid In Preventing Feeding Intolerance and Necrotizing Enterocolitis VLBW Neonates

Start date: March 2014
Phase: Phase 1
Study type: Interventional

The human fetus swallows over 200 ml of amniotic fluid per kilogram of weight each day and such swallowing is essential for normal small bowel development.Growth factors found in the amniotic fluid have been shown to promote proliferation of fetal intestinal cells. As feeding intolerance is a common problem among premature neonates, the investigators will study the role of enteral administration of simulated amniotic fluid solution in prevention of feeding intolerance and NEC in premature neonates.

NCT ID: NCT01530828 Recruiting - Clinical trials for Necrotizing Enterocolitis

IRT in Infants With Intestinal Perforation

Start date: August 2010
Phase: N/A
Study type: Observational

This study is designed to evaluate a novel tool to aid in the diagnosis of intestinal perforation in infants who are at high risk. Analysis of perforation rates of all infants in the three largest participating sites shows that the majority of infants with perforation will do so prior to day of life 21. This study will target the group of infants at highest risk for IP, those with birth weight less than 1000 grams, within the time frame most likely to capture the perforation. Hypothesis: An IRT value exists that can adequately differentiate premature infants with and without intestinal perforation in the first 3 weeks of life.

NCT ID: NCT01441739 Recruiting - Clinical trials for Necrotizing Enterocolitis

Intestinal Failure in Necrotising Enterocolitis

Start date: September 2004
Phase: N/A
Study type: Observational

Necrotizing enterocolitis (NEC) is a severe gastrointestinal disorder with high morbidity and mortality (20-40%), affecting predominantly premature neonates. NEC continues to present a diagnostic challenge to clinicians. The initial clinical manifestations of NEC are non-specific and indistinguishable from other gastrointestinal disorders and sepsis. The first goal of this study is to find and evaluate tests to diagnose NEC at an early stage. For the development of new diagnostic markers, the investigators require knowledge of pathophysiological processes that underlie NEC, which still remain unclear. Therefore, the second goal of this study is to elucidate the etiology of NEC. Furthermore, understanding of the pathophysiology of NEC can offer the possibility to develop new therapeutical treatments.

NCT ID: NCT01315821 Recruiting - Clinical trials for Necrotizing Enterocolitis

Effect of Saccharomyces Boulardii on Necrotizing Enterocolitis in Very Low Birth Weight Infants

Start date: February 2011
Phase: Phase 3
Study type: Interventional

Probiotics are favorable microorganisms that regulate the flora of the gastrointestinal system and stimulate the immune system. Necrotizing enterocolitis incidence is 10-25% in newborn infants whose birth weights are < 1500 gr. Although bifidobacterium and lactobacilli sp. have been used to reduce the incidence of NEC in clinical trials, Saccharomyces boulardii has not been used in the prevention of NEC in very low birth weight infants yet. The objective of this study is to evaluate the efficacy of orally administered S boulardii in reducing the incidence and severity of NEC in very low birth weight infants.

NCT ID: NCT00437567 Recruiting - Clinical trials for Necrotizing Enterocolitis

Prebiotics in the Prevention of Necrotizing Enterocolitis

Start date: July 2009
Phase: Phase 2
Study type: Interventional

Necrotizing enterocolitis (NEC) is the most common gastrointestinal catastrophe affecting 10-15% of premature neonates of <1500 gm. NEC is a disease of the immature intestine, characterized by impaired mucosal barrier function leading to increased gut permeability. We have previously demonstrated a protective effect of probiotic administration against the development of NEC. Others have shown that prebiotics can stimulate natural production of bifidobacteria and lactobacillus in the preterm gut. We have therefore hypothesized that prophylactic administration of prebiotics would also provide protection against necrotizing enterocolitis in the premature neonate, without the potential for sepsis which has been reported on rare occasions with probiotics administration.