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Gallstones clinical trials

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NCT ID: NCT03354065 Completed - Clinical trials for Acute Pancreatitis Due to Gallstones

Inmediate Feeding Tolerance in Acute Pancreatitis

Start date: January 1, 2017
Phase: N/A
Study type: Interventional

Objective: Determine tolerance of immediate oral intake (8 hours posterior to the beginning of treatment) against traditional management (early feeding at 48hr) in patients with mild acute pancreatitis of biliary origin. Double blind, randomized clinical trial

NCT ID: NCT03193177 Completed - Chronic Disease Clinical Trials

A Retrospective and Prospective Cohort Study of the 21-day Fasting-like Diet in Patients With Metabolic and Autoimmune Diseases

Start date: June 20, 2017
Phase:
Study type: Observational

Effectiveness of fasting or fasting-mimicking diet has been proved an effective approach to treat metabolic and autoimmune diseases in mice. However, clinical trials performing prolonged fasting with more than 7 days have not been reported. Investigators conduct an open label, phase I/II clinical trial to evaluate the safety and effectiveness of the 21-day fasting-like diet in the treatment of metabolic and autoimmune diseases.

NCT ID: NCT03180229 Completed - Cholelithiasis Clinical Trials

Granisetron Effect on Hemodynamic Changes in Laparoscopic Cholecystectomy

lap
Start date: May 29, 2017
Phase: Phase 4
Study type: Interventional

Propofol is one of the most commonly used anesthetic agents because of its ability to induce rapid and reliable collection. However, hypotension and injection pain in the induction are the most common complications. After induction of propofol; The cardiovascular system depresses, resulting in a drop in blood pressure due to decreased cardiac output and systemic vascular resistance. This may also contribute to the reduction of sympathetic tone activity in the central way, and slight reduction in the number of pulses that develop as a result of increasing vagal activity. İn order to attenuate these hemodynamic undesired effects caused by propofol, various agents were tried such as atropine, ephedrine, volume replacement ringer lactate, ketamine. Ondansetron and granisetron, which are used for postoperative nausea and vomiting prophylaxis, have been used as such. Therefore, ondansetron and granisetron were preventing hypotension induced by post-spinal and general anesthesia induction. The investigator also tried to demonstrate the effect of granisetron, another serotonin type 3 (5-HT3) receptor antagonist for postoperative nausea and vomiting prophylaxis, on induction hypotension and intubation quality after propofol induction in this study

NCT ID: NCT03168555 Completed - Cholelithiasis Clinical Trials

Changes in Bile Acid Homeostasis and Stool Habits After Cholecystectomy

BACH
Start date: June 22, 2017
Phase: Phase 4
Study type: Interventional

Investigate serial plasma samples of fibroblast growth factor 19 (FGF19) after oral stimulation with chenodeoxycholic acid in the same subjects before and after elective cholecystectomy

NCT ID: NCT03154164 Completed - Cholecystolithiasis Clinical Trials

Study on the Learning Curve for Fundus First With Ultrasonic Tissue Coagulation in Elective Cholecystectomy

LEFFE
Start date: May 1, 2017
Phase:
Study type: Observational

The present study aims at analyzing the learning curve for fundus first with the ultrasonic tissue coagulation dissection technique in elective cholecystectomy. Patients included in the study are planned for an elective cholecystectomy, on the basis of the gallstone disease. All participating surgeons have experience of the traditional approach with electrocautery. The operation time as well as the surgeons own evaluation of difficulty and performance are noted. Selected films are analyzed by independent surgeons with experience of the fundus first technique. The Swedish registry of gallstone surgery and ERCP (GallRiks) are used to record the intra and postoperative complication rate.

NCT ID: NCT03118973 Completed - Biliary Obstruction Clinical Trials

Evaluation of Efficacy and Safety of Goff Transpancreatic Septotomy vs. Double Wire Technique for Achieving Biliary Access in Technically Challenging ERCPs

Start date: September 27, 2016
Phase: N/A
Study type: Interventional

Randomized, prospective study evaluating efficacy and safety of Goff transpancreatic septotomy vs. double wire technique for achieving biliary access in patients who fail initial cannulation at ERCP.

NCT ID: NCT03059745 Completed - Cholecystitis Clinical Trials

Use of Robotics for Cholecystectomy; Retrospective Review of Outcomes, Set Up and Learning Curves

Start date: June 2004
Phase:
Study type: Observational

Comparing the use of surgical robotics during a Cholecystectomy, comparing different platforms and approaches (multi port verses single port).

NCT ID: NCT02967926 Completed - Clinical trials for Cholangitis, Sclerosing

Digital SpyGlass Confirmed Common Bile Duct Stones Clearance Without Fluoroscopy

Start date: December 2015
Phase: Phase 3
Study type: Interventional

This study aim to evaluated the effectiveness of Digital SpyGlass Cholangioscopy to facilitate common bile duct stone removal without fluoroscopy

NCT ID: NCT02947256 Completed - Gallstones Clinical Trials

Laparoscopic Cholecystectomy With Retro-infundibular Approach

Start date: July 2013
Phase: Phase 2
Study type: Interventional

Aimed to evaluate laparoscopic cholecystectomy by retro-infundibular (RI) approach compared to standard laparoscopic cholecystectomy (SLC) in difficult cases with scarred chole-cystohepatic (Calot's) triangle.

NCT ID: NCT02909595 Completed - Biliary Calculi Clinical Trials

Balloon Catheter vs. Basket Catheter for Endoscopic Bile Duct Stone Extraction

Start date: November 2014
Phase: Phase 4
Study type: Interventional

Endoscopic bile duct stone (BDS) removal is a well-established treatment; however, the preference for basket or balloon catheters for extraction is operator-dependent It is reported that complete endoscopic treatment with a single catheter is more likely when choosing a balloon catheter over a basket catheter for extraction of BDSs≤10mm. However, a study comparing the two catheter types in patients with periampullary diverticulum has not been performed, and there is no strong basis on which to recommend the balloon catheter as a first-line stone removal device. The investigators therefore conducted a multicenter prospective randomized trial to compare catheter performance in patients with periampullary diverticulum.