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Esophageal Fistula clinical trials

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NCT ID: NCT04507295 Not yet recruiting - Clinical trials for Congenital Diaphragmatic Hernia

Cerebral Blood Flow in Neonates During Thoracoscopic Surgeries

Start date: August 8, 2020
Phase: N/A
Study type: Interventional

the aim of this study is to compare the effect of different modes of mechanical ventilation by using volume-controlled ventilation and pressure-controlled ventilation on cerebral blood flow monitored by cerebral oximetry during thoracoscopic surgeries in neonates.

NCT ID: NCT04183621 Recruiting - Clinical trials for Esophageal Atresia With Tracheoesophageal Fistula

Swallowing, Feeding and Eating in Children Born With Oesophageal Atresia/Trache-oesophageal Fistula (OA/TOF)

SaFE
Start date: December 15, 2020
Phase:
Study type: Observational

How does oesophageal atresia/trache-oesophageal fistula affect feeding and swallowing in the first year of life? Approximately 150 babies a year are born with oesophageal atresia and/or trache-oesophageal atresia. Oesophageal atresia occurs when the oesophagus (food pipe) fails to join up during early foetal development. Trache-oesophageal fistula describes an abnormal connection that forms between the oesophagus and trachea (wind pipe). When the baby feeds, milk cannot pass into the stomach but can pass into the lungs. Surgery is needed within the first few days of life and is extremely successful, with 90-95% of babies surviving. However, approximately 50-80% of babies will have ongoing feeding or swallowing difficulties resulting in choking, chest infections and pneumonia. They can also lead to food refusal, distress at mealtimes and parental anxiety. Currently there is limited understanding of: - the exact nature of the feeding and swallowing difficulties - the risk factors for developing difficulties - the impact on parents. This study will address these issues through two complimentary projects: Project 1: A study of swallow physiology Babies with oesophageal atresia and/or trache-oesophageal fistula who have surgery at Great Ormond Street Hospital will be invited to have a detailed swallow assessment using videofluoroscopy (video x-ray) and high resolution impedance manometry (a pressure monitor) at 2-4 months of age and at 8-12 months of age. Results will be compared to parent report of feeding at 1 year old. Project 2: A study of the impact on parental well-being This study will be carried out in conjunction with the 'TOFS' support group. A Facebook page will be used to carry out an online forum. Parents of any child who has had TOF/OA will be invited to share their experiences of establishing feeding. This information will be used to develop a questionnaire to look at how wide-ranging these experiences are.

NCT ID: NCT03832959 Recruiting - Atrial Fibrillation Clinical Trials

Esophageal Damage Protection During Pulmonary Vein Ablation. Pilot Study.

Start date: March 11, 2019
Phase: N/A
Study type: Interventional

Catheter ablation of atrial fibrillation with electrical isolation of the pulmonary veins in the left atrium carries risk of esophagus thermal lesion. EnsoETM is a device . This study evaluates the benefit of using the EnsoETM, a device device for esophageal temperature adjustments, during catheter ablation of atrial fibrillation. Half of participants will undergo esophageal temperature adjustment during pulmonary vein catheter ablation, while the other half will undergo catheter ablation with no esophageal temperature adjustment.

NCT ID: NCT02751333 Withdrawn - Esophageal Fistula Clinical Trials

Esophageal Stent Migration With Endoscopic Suture Fixation Compared to Standard Deployment

Start date: March 2016
Phase: Phase 2
Study type: Interventional

Esophageal stents are commonly used for benign esophageal pathology, especially strictures or esophageal mucosal defects such as leaks, fistulae, or perforations. The major limiting factor to stent placement is the high migration rate of the stent. Investigators are trying to prospectively evaluate the efficacy of endostitch in preventing stent migration in benign esophageal disease in comparison with standard, fully covered self-expanding metal stents (FCSEMS) placement without fixation.

NCT ID: NCT02665442 Not yet recruiting - Atrial Fibrillation Clinical Trials

Retracting the Esophagus During AF Ablation

EsoSure
Start date: January 2016
Phase: N/A
Study type: Interventional

This Study is designed to determine the outcome and effect of implementation of Esophageal Stylet as a strategy to minimize the risk of esophageal injury during the atrial fibrillation catheter ablation procedure.

NCT ID: NCT01900691 Completed - Clinical trials for Esophageal Neoplasms

Removal of the Evolution® Esophageal Stent - Fully Covered

CLARITY
Start date: September 2013
Phase: N/A
Study type: Interventional

The CLARITY study is a clinical trial approved by US FDA to study the removal of the Evolution® Esophageal Stent-Fully Covered in malignant and benign indications.

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: NCT01287312 Recruiting - Clinical trials for Tracheo Esophageal Fistula

Trichloroacetic Acid for Endoscopic Tracho-esophageal Fistula Repair

Start date: January 2011
Phase: N/A
Study type: Interventional

Today Endoscopic repair of recurrent Tracheesophageal fistula (TEF) is a safe procedure. Using Trichlosiacetic acid 50% (TCA) for endoscopic aplication of the fistula was reported with a good results ( 4 cases). There were no serious advers effects. The investigators want to use also TCA 50% for endoscopic repair in children with recurrent TEF.

NCT ID: NCT01153061 Terminated - Clinical trials for Acquired Tracheo-esophageal Fistula

Endoscopic Closure of Tracheoesophageal Fistulas With Occluder Device

TEFGoreHelex
Start date: June 2010
Phase: Phase 4
Study type: Interventional

Endoscopic closure of tracheoesophageal fistulas with a device used for closure of cardiac septal defects.