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Drainage clinical trials

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NCT ID: NCT06141044 Not yet recruiting - Drainage Clinical Trials

Prophylactic Abdominal Drainage vs no Drainage After Distal Pancreatectomy

PANDREAS
Start date: January 2024
Phase: N/A
Study type: Interventional

Postoperative pancreatic fistula (POPF) is a major source of morbidity and mortality after pancreatic resection, especially after distal pancreatectomy (PD). Today, POPF remains one of the main causes of hospital length of stay and healthcare costs. Numerous surgical techniques have been tested to reduce its incidence without success, so the current standard for the management of POPF, and the avoidance of associated complications, is intraoperative drain placement. However, surgically placed drains are not without risk. In recent years many studies, mostly retrospective, have attempted to determine whether omission of prophylactic drainage is associated with increased morbidity. These studies suggest that patients may benefit from not having a drain placed. This evidence challenges standard practice and the debate of whether or not to place a drain after distal pancreatectomy remains open. The investigators designed a prospective multicentre randomised non-inferiority study to determine whether prophylactic intraoperative drainage is associated with a lower morbidity rate after distal pancreatectomy.

NCT ID: NCT05688137 Not yet recruiting - Clinical trials for Liver Transplant; Complications

Abdominal Drainage in the Postoperative Period of Liver Transplantation (DRALIT)

DRALIT
Start date: January 15, 2023
Phase: N/A
Study type: Interventional

Classically, in the postoperative period of liver transplantation (LT), abdominal drainage has been used as a way to make the early diagnosis of hemorrhages, bile leaks and other postsurgical complications, as well as an evacuation route for ascites. The use of it routinely is currently under discussion due to the morbidities associated with its use.

NCT ID: NCT05267860 Completed - Clinical trials for Laparoscopic Cholecystectomy

The Efficacy and Safety of Using Prophylactic Abdominal Drainage After Cholecystectomy

Start date: February 1, 2022
Phase: N/A
Study type: Interventional

Investigators want to assess the safety and efficacy of using abdominal drainage with not using any drainage, by estimating different outcomes after laparoscopic cholecystectomy for different reasons. Patients are seen at the Accident and Emergency Department or in the surgical wards at Aleppo University Hospital (AUH) over 12 months period.

NCT ID: NCT04931576 Recruiting - Thyroid Cancer Clinical Trials

No Drainage During Transoral Endoscopic Thyroidectomy Vestibular Approach(TOETVA)

Start date: July 1, 2021
Phase: N/A
Study type: Interventional

This study evaluates the viability and safety of no drainage tube placement during transoral endoscopic thyroidectomy vestibular approach in treatment of patients with papillary thyroid carcinoma.

NCT ID: NCT04207671 Not yet recruiting - Drainage Clinical Trials

Improved Drainage Strategy for Patients With Lung Wedge Resection

Start date: March 2020
Phase: N/A
Study type: Interventional

This study evaluates the viability and safety of two-lumen catheterization versus complete omission of chest tube in patients with lung wedge resection. Half of participants will receive complete omission of chest tube, while the other half will receive a two-lumen central venous catheterization along the midclavicular line, second intercostal space for remedial gas-remove.

NCT ID: NCT03231072 Completed - Pleural Effusion Clinical Trials

Pleural Effusion Drainage in Mechanically Ventilated Patients Monitored by EIT

Start date: January 31, 2017
Phase: N/A
Study type: Interventional

Evacuation of pleural effusion (PE) represents a disputable therapy in mechanically ventilated patients. Patients on mechanical ventilation indicated by the physician to pleural fluid evacuation will be monitored throughout the procedure by electrical impedance tomography (EIT) and concurrently end-expiratory lung volume (EELV) will be measured in order to describe impact of PE evacuation on aeration and ventilation of the lungs.

NCT ID: NCT03055676 Completed - Clinical trials for Pancreaticoduodenectomy

Prospective Multicenter Trial of Early Versus Late Drain Removal After Pancreaticoduodenectomy

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

The aim of this randomized prospective multicenter study is to demonstrate the hypothesis that early removal of drain could reduce the incidence of major complications (grade 2-4) after pancreaticoduodenectomy (PD) , when compared with later removal of drain.

NCT ID: NCT02845258 Recruiting - Clinical trials for Pancreatic Pseudocyst

Treatment of Pancreatic Pseudocysts by Endoscopic Ultrasound-guided Drainage

Start date: January 2006
Phase:
Study type: Observational

Patients may evolve pseudocysts of the pancreas secondary to a severe pancreatitis. In case of a symptomatic or infected pseudocyst, a therapeutic drainage of the cyst is indicated. In modern medicine the preferred way to perform such a drainage is by the means of endoscopic ultrasound (EUS). It is not precisely elucidated how this EUS-procedure should be performed in different scenarios. The cyst appearance and the drainage stents and/or technique may impact the clinical outcome. This study is a prospective, single-center observational study on the outcome after EUS-guided drainage of pancreatic pseudocysts.

NCT ID: NCT02158299 Recruiting - Clinical trials for Postoperative Complications

Contrast The Role of Avitene And OK-432 in Reducing Seroma Formation After Axillary Lymphadenectomy for Breast Cancer

Start date: October 2013
Phase: Phase 4
Study type: Interventional

After Axillary lymphadenectomy for breast cancer there are not few patients showed seroma formation and it can not be ignored.Investigators aimed to study two new methods of application of Microfibrillar Collagen Hemostat Flour and OK-432 to reduce seroma formation and to verify the efficacy and safety of these two applications.Try to prove them as beneficial supplements for axillary lymphadenectomy of breast cancer.

NCT ID: NCT01896219 Completed - Ablation Clinical Trials

CTNAV II : Multicentric Evaluation of IMACTIS-CT Navigation System

Start date: December 2013
Phase: N/A
Study type: Interventional

Estimate the medical service of a system of navigation (IMACTIS-CT®)in terms of SAFETY, EFFICIENCY and PERFORMANCE, in comparison with the reference method during gestures of interventional radiology under scan in the thoraco-abdominal level.