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Hernia, Diaphragmatic clinical trials

View clinical trials related to Hernia, Diaphragmatic.

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NCT ID: NCT02466451 Completed - Clinical trials for Diaphragmatic Hernia

Study in Children With the Diagnosis of Congenital Diaphragmatic Hernia (CDH) and Oesophageal Atresia (EA)

CDH-EA
Start date: March 2014
Phase: N/A
Study type: Observational

Observational longitudinal study in children operated at birth on diaphragmatic hernia and/or oesophageal atresia : assessment of lung function parameters; assessment of quality of life and cognitive development; assessment of stress parenting and strategies of adaptation.

NCT ID: NCT02453750 Completed - Clinical trials for Congenital Diaphragmatic Hernia

Airway Inflammation in Congenital Diaphragmatic Hernia Patients

Start date: February 2012
Phase: N/A
Study type: Interventional

We propose to examine Congenital Diaphragmatic Hernia (CDH) patients for evidence of airway inflammation as a first step to characterize the reported bronchodilator responsiveness. Airway biopsy studies are invasive and thus we propose to perform induced sputum studies to document the amount and type of inflammation present. Another ancillary non-invasive measure of airway inflammation that we will use is exhaled nitric oxide (NO). The primary objective of this study is to determine if CDH patients have any evidence of airway inflammation. The hypothesis of this study is that children with CDH do not have evidence of airway inflammation associated with bronchodilator responsiveness. Based on this information, treatment for CDH patients will hopefully be more accurate and appropriate for their specific needs.

NCT ID: NCT02364843 Terminated - Clinical trials for Diaphragmatic Hernia

A Physiological Study to Determine the Enteral Threonine Requirements in Infants Aged 1 to 6 Months

INFORALTHR
Start date: February 2016
Phase: N/A
Study type: Interventional

This is the 5th in a series of physiological studies to determine the amino acid requirements of infants. There have been 4 studies to determine tyrosine, methionine, threonine and lysine requirements in infants when they are fed by parenterally (intravenously). Due to the new requirements of Health Canada for preparation of parenteral solutions, the investigators are starting the phase of the study that determines the enteral (oral) intake of threonine in 1 - 6 mo infants in the interim.

NCT ID: NCT02175264 Completed - Clinical trials for Isolated Non Syndromic Left CDH With Postero Lateral Diaphragmatic Defect With Good Perinatal Outcome

Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia

HCD GENE
Start date: June 2014
Phase: N/A
Study type: Observational

In isolated congenital diaphragmatic hernia (CDH), recurrent risk is low suggesting the occurrence of novo mutations (dominant or recessive). Our objective is to test this hypothesis by combining the search for pathogenic genomic alteration and intragenic mutations through whole exome sequencing in a homogenous group of patients.

NCT ID: NCT02137018 Active, not recruiting - Incisional Hernia Clinical Trials

"Nanotechnologies Applied to General Surgery and Emergency Surgery: Buckypaper as a New Fixing Method for Prosthetic Materials for the Treatment of Hernia and Incisional Hernia in Laparotomy and Laparoscopic

36P
Start date: March 2013
Phase: Phase 1/Phase 2
Study type: Interventional

"Nanotechnologies applied to General Surgery and Emergency Surgery: The Buckypaper as a new fixing method for prosthetic materials in the treatment of abdominal wall hernias, diaphragmatic hernias, diaphragmatic rupture, incisional hernia and abdominal wall disaster in laparotomy procedure and laparoscopic procedures". Experimentation on breed pig Lantrace ANIMAL MODEL.

NCT ID: NCT02033772 Completed - Clinical trials for Congenital Diaphragmatic Hernia

Prospective Data Collection of Patients < 6 Months of Age Undergoing Thoracoscopic Surgery

Start date: August 2013
Phase: N/A
Study type: Observational

The study is primarily a descriptive study examining the physiological, ventilatory, surgical, and recovery effects of patients ≤ 6 months of age who undergo thoracoscopic surgery and to determine the accuracy of transcutaneous CO2 (TC-CO2) and end-tidal CO2 (ET-CO2) during high frequency oscillatory ventilation (HFOV) and thoracoscopic procedures.

NCT ID: NCT01731509 Not yet recruiting - Clinical trials for Congenital Diaphragmatic Hernia

Early FETO for Severe Congenital Diaphragmatic Hernia

Start date: June 2014
Phase: Phase 2
Study type: Interventional

Congenital diaphragmatic hernia (CDH) is associated high mortality and morbidity, mainly in those cases with severe forms where there are extremely reduced lung volumes, liver herniation and decreased abnormal pulmonary vascularization. Fetal endoscopic tracheal occlusion performed between 26 and 30 weeks (standard FETO) has been shown to increase fetal pulmonary size and vascularity, and to improve infant survival in isolated severe CDH. Fetal pulmonary response followed FETO can be used to predict outcome and is dependent on the size of the fetal lung prior to the procedure. We hypothesize that performing an earlier FETO, between 22-24 weeks, fetuses with severe form of CDH will have a better fetal pulmonary response and higher chance of surviving.

NCT ID: NCT01467245 Completed - Clinical trials for Congenital Diaphragmatic Hernia

Open or Keyhole Surgery Through the Chest for Newborn Babies: Effect on Blood Gases

CO2
Start date: August 2009
Phase: N/A
Study type: Interventional

This is a pilot randomised controlled trial comparing open versus thoracoscopic surgery for repair of oesophageal atresia with tracheo-oesophageal fistula or congenital diaphragmatic hernia in neonates. Thoracoscopic surgery involves insufflation of carbon dioxide into the thoracic cavity and may therefore cause hypercapnia and acidosis.

NCT ID: NCT01302977 Unknown status - Clinical trials for Congenital Diaphragmatic Hernia

Fetal Tracheal Occlusion in Severe Diaphragmatic Hernia: a Randomized Trial

BRAFETO
Start date: May 2008
Phase: Phase 2
Study type: Interventional

The neonatal mortality rate in cases with severe isolated congenital diaphragmatic hernia is higher than 90% due to severe pulmonary hypoplasia. Many studies have suggested that fetal tracheal occlusion may increase lung volumes and therefore reducing the risk for severe pulmonary hypoplasia and by consequence the risk for neonatal death. The main objective of the present study is to evaluate if fetal tracheal occlusion improves survival rate in those cases that are followed in our hospital, by conducing a randomized trial.

NCT ID: NCT01243229 Completed - Clinical trials for Congenital Diaphragmatic Hernia

Genetic Analysis of Congenital Diaphragmatic Disorders

Start date: October 2010
Phase:
Study type: Observational

The purpose of this study is to understand the genetic causes of congenital diaphragmatic disorders (CDD), namely congenital diaphragmatic hernia (CDH), eventration and hiatal hernia. Specifically, the investigators plan to: 1. Ascertain informative families and sporadic cases with congenital diaphragmatic disorders and obtain appropriate phenotypic data and genetic material (peripheral blood and/or diaphragm tissue sample). 2. Localize the gene(s) for CDD to specific chromosomal segments using linkage analysis, and determine the role of somatic mutations in CDD. 3. Isolate and characterize genes involved in the pathogenesis of CDD. 4. Develop molecular markers that will facilitate accurate diagnosis (including prenatal diagnosis) and permit correlation of phenotypic variation with specific mutations. 5. Compare RNA-sequencing from tissue samples of children without CDH to those children with CDH.