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Digestive System Abnormalities clinical trials

View clinical trials related to Digestive System Abnormalities.

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NCT ID: NCT03615495 Completed - Esophageal Atresia Clinical Trials

Flourish™ Pediatric Esophageal Atresia

Start date: November 5, 2018
Phase:
Study type: Observational

This study is continued evaluation of the safety and probable benefit of the Flourish Pediatric Esophageal Atresia device through the Humanitarian Device Exemption (HDE) pathway.

NCT ID: NCT03603093 Completed - Endoscopy Clinical Trials

A Multicenter Survey of the Indications for Esophagogastroduodenoscopy (EGD)

Start date: December 24, 2018
Phase:
Study type: Observational

Esophagogastroduodenoscopy (EGD) become more and more common in diagnosing gastroenterology diseases. The investigators want to find which symptoms can support for positive endoscopic findings through this multicenter study.

NCT ID: NCT03362450 Completed - Midgut Volvulus Clinical Trials

Prenatal Diagnosis of Antenatal Midgut Volvulus: Specific Ultrasound Features

Start date: January 1, 2006
Phase: N/A
Study type: Observational

Objective: The small bowel volvulus is a rare cause of intestinal obstruction which may occur in utero and whose prenatal diagnosis is difficult.Sonographic signs are mainly indirect and non specific.The aim of this study is to present a retrospective analysis of prenatal sonographicfindings in fetal segmental midgut volvulus.Thanks to this series the investigators could highlight the more specifics signs of the volvulus included a new pattern.

NCT ID: NCT03356314 Completed - Clinical trials for Intestinal Malrotation

Prenatal Ultrasound Screening of Intestinal Malrotation With a Higher Risk of Volvulus

VOLMES
Start date: January 1, 2017
Phase:
Study type: Observational

The aim of this study was to assess the value of an unusual relative position of the superior mesenteric artery (SMA) and vein (SMV) to screen intestinal malrotation with a higher risk of volvulus. First, feasibility study was done to prove the reproducibility of ultrasound in diagnosis of anormal mesenteric vessels position. A systematic screening of the mesenteric vessels position was performed at each pregnancy required ultrasound. When the fœtus had an unusual position of the mesenteric vessels, an MRI was suggested between 30 and 35 GA and the couple met the pediatric surgery team. Few days after birth, an abdominal ultrasound was achieved as well as a barium enema and upper gastrointestinal. If there were a hight probability of malrotation with a higher risk of volvulus, a prophylactic surgery was proposed. The children were flollowed up during 1 year.

NCT ID: NCT03157011 Completed - Sjogren's Syndrome Clinical Trials

Evaluation of the Prevalence of Functional Digestive Disorders During Primary Sjögren Gougerot Syndrome

GASTRO-SGS
Start date: July 17, 2017
Phase: N/A
Study type: Interventional

the investigators propose to carry out a prospective study consisting of a systematic research of digestive symptoms in patients with SGSp with the validated Global symptom score (GSS) questionnaire, which allowed to grades severity of 10 digestive symptoms (absent, mild, moderate, or severe), asthenia and fever.

NCT ID: NCT02789514 Completed - Clinical trials for Digestive System Abnormalities

A Survey of the Indications for Esophagogastroduodenoscopy (EGD) in Children's Hospital of Fudan University

Start date: July 2016
Phase: N/A
Study type: Observational

Esophagogastroduodenoscopy (EGD) become more and more common in diagnosing gastroenterology diseases. The investigators want to find which symptoms can support for positive endoscopic findings.

NCT ID: NCT02530983 Recruiting - Esophageal Cancer Clinical Trials

Mayo Clinic Upper Digestive Disease Survey

UDD
Start date: August 2015
Phase:
Study type: Observational

The Mayo Clinic Conduit Report Card Questionnaires have been created in order to have a consistent evaluation tools for patients undergoing esophageal reconstruction or treatment or patients that are experiencing an upper digestive disease in order to standardize and validate outcome measures. Data will be used to establish the validation of the questionnaires/survey. Data will also lead to the establishment of "normal" or expected scores for patients undergoing each type of esophagectomy procedure and for upper digestive diseases. Data will contribute to creating treatment algorithms for symptom management for upper digestive diseases and for post-operative complications and symptoms as well as contribute to pre-operative education.

NCT ID: NCT01451307 Completed - Clinical trials for Digestive System Abnormalities

Follow-up of Children With Gastrointestinal Malformations and Postnatal Surgery

FraMal
Start date: September 2011
Phase: N/A
Study type: Observational

The aim of this single center study is to measure the impact of standardized neonatal pediatric surgeries due to gastrointestinal malformations on the children's motor and cognitive development and psycho-emotional competence. To measure the neurodevelopment, the children will be tested with the Bayley Scales of Infant Development II Assessment.

NCT ID: NCT00780117 Completed - Clinical trials for Sacrococcygeal Teratoma

Characterization of At-risk Population for Pre-sacral Tumor in CURRARINO Syndrome

Currarino
Start date: June 2008
Phase: N/A
Study type: Observational

Contribute to support hypothesis of relationships between genes involve in oncogenesis and those involve in embryological development.

NCT ID: NCT00392977 Completed - Clinical trials for Necrotizing Enterocolitis

Brain Manganese Deposition in High Risk Neonates

Start date: August 2006
Phase: N/A
Study type: Observational

Excessive exposure to manganese (Mn) results in Mn deposition in the brain causing adverse neurological effects. Sick infants requiring parenteral nutrition (PN) may be at increased risk of Mn neurotoxicity because neonatal PN solutions contain high concentrations of Mn. This proposal will investigate brain deposition of Mn, a paramagnetic element, by magnetic resonance (MR) imaging in preterm and term neonates receiving Mn-supplemented PN and gestational age-matched control infants. The goals of this project are to identify neonatal populations that are at increased risk of excessive brain Mn deposition based on their gestational age, iron status, hepatic function and dietary Mn intake, and to make evidence-based recommendations for appropriate Mn supplementation and monitoring of infants receiving PN.