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Bile Leak clinical trials

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NCT ID: NCT04477005 Completed - Bile Leak Clinical Trials

Archimedes Bio-degradable Bile Duct Stent Study

ABBS
Start date: November 11, 2020
Phase:
Study type: Observational

This is a prospective observational cohort study to assess the utility of bio-degradable bile duct stent in the drainage of bile duct. All consecutive patients who will undergo ERCP procedure for bile leaks and patients with bile duct stones and intact gall bladder will be recruited to the study. The planned sample size is 53 and patients will be followed up for 180 days. The primary objective is to assess the utility of biodegradable bile duct plastic stents in the drainage of bile duct. The secondary Secondary objectives are To assess 1. Technical success of biodegradable stents 2. Complications 3. Patient related cost savings (Time off work, travel time for the patient) 4. Hospital related cost savings (Repeat procedure costs, follow up appointments)

NCT ID: NCT04451447 Completed - Bile Leak Clinical Trials

White Test in Intra-operative Detection of Donor Biliary Leak in LDLTx.

LDLTx
Start date: March 20, 2019
Phase: N/A
Study type: Interventional

Biliary leak is a common complication after partial liver resection in living donor liver transplant. It debases the quality of the postoperative course and affects morbidity and mortality. Detecting and localizing sites of biliary leak intraoperatively through bile leakage testing is important as it helps in detection of bile leaking points on the cut surface and decrease post-operative bile leak. In this study we will assess the efficacy and sensitivity of using White test in comparison to conventional saline test in detecting intra operative bile leakage in liver donor. The White test uses fat emulsion (SMOFLIPID), which is a lipid emulsion with a lipid content of 0.2 grams/mL in 100 mL, 250 mL, and 500 Ml that is normally used for parenteral nutrition, for localization of bile leakage. The use of fat emulsion in bile leakage tests does not require special equipment, contaminate the wound, cause allergic reaction or damage the bile duct and surrounding tissues.

NCT ID: NCT03673033 Completed - Biliary Stricture Clinical Trials

Biliary Complications in Live Donor Liver Transplantation

Start date: March 10, 2018
Phase:
Study type: Observational [Patient Registry]

The study was designed as a prospective cohort study. The effects of hot and cold ischemic times during live donor liver transplantation on postoperative 1-3 and 6 month follow up biliary complications will be investigated.

NCT ID: NCT02056028 Completed - Hepatectomy Clinical Trials

Bile Leak After Liver Surgery

Start date: January 2004
Phase: N/A
Study type: Observational [Patient Registry]

The definition of biliary fistula is heterogeneous and the more accepted is that proposed by the ISGLS. We devised a precise definition of post-resectional biliary fistula and a well-established policy both for its disclosure and management.Aim was the validation of our definition, and management of biliary fistula after hepatic resection in a large prospective cohort of patients and its comparison with that of the International Study Group of Liver Surgery (ISGLS).