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Chylothorax clinical trials

View clinical trials related to Chylothorax.

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NCT ID: NCT05683444 Completed - Lymphatic Diseases Clinical Trials

Octreotide Improves Human Lymphatic Fluid Transport a Translational Trial

Start date: July 1, 2020
Phase: Early Phase 1
Study type: Interventional

This study aims to investigate whether octreotide, a medication used off-label to treat chylothorax, has a direct effect on human lymphatic drainage. To study the effects of octreotide, the researchers conducted a pre-clinical experiment using human lymphatic vessels mounted in a myograph chamber and a clinical experiment in which a double-blinded, randomized, cross-over trial was conducted in 16 healthy adults. The results of the study will be used to determine the role of octreotide in the treatment of chylothorax and other lymphatic disorders.

NCT ID: NCT03292757 Completed - Esophageal Cancer Clinical Trials

FLOTOR Pilot Study

FLOTOR
Start date: December 20, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

This is a non-randomised study assessing the technique of using indocyanine green as a fluorescent dye to highlight the thoracic duct during oesophectomy.

NCT ID: NCT02577419 Completed - Chylothorax Clinical Trials

Optimizing Growth in Infants Receiving Modified Fat Breast Milk for the Treatment of Chylothorax

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

Breast milk is the reference normative standard for infant feeding. When an infant is diagnosed with chylothorax, provision of breast milk must be temporarily discontinued due to the presence of long chain triglycerides (LCT) that contribute to persistent chylous drainage. In its place, the infant is prescribed a therapeutic formula high in medium chain triglycerides (MCT) as treatment for chylothorax. Families and health care providers are interested in using breast milk, in a modified fat form, as treatment for chylothorax instead. This study will assess growth in infants receiving one of two nutrient enriched modified fat breast milk (MFBM) treatments for chylothorax. If either of the proposed nutrient enrichment methods support growth, MFBM will become a standard chylothorax treatment option for infants at SickKids.

NCT ID: NCT02143557 Completed - Chylothorax Clinical Trials

Dietary Treatment of Infants With Chylothorax

Start date: January 2008
Phase: N/A
Study type: Interventional

Chylothorax occurs in ~3 to 5 % of infants undergoing cardiac surgery. Standard treatment requires discontinuation of breast milk feeding, due to the abundance of long chain triglycerides, and transition to a medium chain triglyceride (MCT) based formula. Objective: To determine the effectiveness of fat-modified breast milk (MBM) for the treatment of chylothorax compared with MCT-formula. Hypothesis: The investigators primary hypothesis was that infants fed MBM would have more chyle drainage in the first 5 days after diagnosis compared to infants fed an MCT based formula which is the current standard of care. Design: Infants with chylothorax were eligible. Treatment infants (n=8) received mother's own milk that had been modified by removing the fat layer via centrifugation and adding MCT and nutrients to provide 67 kcal/mL and 11 g/100 mL protein (MBM group). Control infants (n=8) received an MCT-formula (MCT group). The feeding intervention was a minimum of 6 weeks after chest tube removal per The Hospital for Sick Children standard chylothorax treatment protocol. Outcome measures collected included chyle drainage from chest tubes, weight, length and head circumference measurements and estimated energy and nutrient intake.

NCT ID: NCT01673165 Completed - Clinical trials for Chylous Pleural Effusion Following Cardiothoracic Surgery

Fortified Skimmed Mother's Milk in the Management of Chylothorax

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

The purpose of this study is to determine if the use of fortified skimmed mother's milk is a safe alternative to specialized formula in the treatment of chylothorax following cardiothoracic surgery.

NCT ID: NCT01522885 Completed - Pneumothorax Clinical Trials

KatGuide Method Versus Conventional Method at Insertion of Chest Tube

KatGuide
Start date: April 2012
Phase: Phase 3
Study type: Interventional

The purpose of this study is to investigate whether if KatGuide (a new developed medical device) improves the placing of a large bore chest tube in the pleural cavity compared to the conventional method.