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Fistula clinical trials

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NCT ID: NCT04136522 Recruiting - Recurrence Tumor Clinical Trials

Usefulness of the Artery First Approach in Pancreatic Cancer Surgery

Start date: January 10, 2020
Phase: N/A
Study type: Interventional

This study is aimed to evaluate difference of the 2 year recurrence free survival after pancreaticoduodenectomy for pancreatic cancer between artery-first approach and conventional procedure groups.

NCT ID: NCT04119700 Recruiting - Anal Fistula Clinical Trials

Fistulectomy and Primary Sphincter rEconstruction vs. endorectaL Advancement Flap in the Treatment of High Anal Fistulas

SELF
Start date: November 4, 2017
Phase: N/A
Study type: Interventional

The optimal method of surgical treatment of complex anorectal fistulas has not been found yet. The aim of this study is to compare two techniques in treatment of high anorectal fistulas. This study purpose to demonstrate that the fistulectomy with dissection from 1/3 to 2/3 of the height of the sphincter complex with primary suturing is technically simpler, equally effective and safe in comparison with muco-muscular endorectal advancement flap.

NCT ID: NCT04058236 Recruiting - Pancreatic Cancer Clinical Trials

Glycocalyx Levels in Patients Undergoing Pancreatectomy

Start date: August 15, 2019
Phase: Phase 4
Study type: Interventional

Background: On the surface of every healthy cellular membrane resides a layer known as the glycocalyx. This structure consists of extracellular domains of receptor, adhesion and transmembrane molecules such as syndecan-1 covalently bound to highly negatively charged glycosaminoglycans, heparan sulfates. It has a principal role to maintain wall integrity, avoid inflammation and tissue oedema in vessels but in contrast, glycocalyx is robust and elevated on cancer cells. This study examines whether the endothelial glycocalyx layer is preserved in patients undergoing pancreatectomy with human albumin 5% vs. gelofusine in a restrictive goal directed fluid regime perioperatively for the first 24hours. Degradation of glycocalyx will be investigated by analyzing basic levels of the core protein syndecan-1 and heparan sulfates with post-operative samples.

NCT ID: NCT04034433 Recruiting - Clinical trials for Arteriovenous Fistula

Exercise Program for Arteriovenous Fistula Maturation

FAVULOUS
Start date: October 4, 2019
Phase: N/A
Study type: Interventional

Arteriovenous fistula (AVF) is the recommended vascular access for chronic hemodialysis, as it is associated with less mortality and better patency than arteriovenous graft (AVG) or central venous catheter (CVC). Unfortunately, AVF suffers from a high failure rate, due, in part, to poor venous diameter. The aim of this study is to investigate whether a perioperative handgrip training can improve the diameter of AVF in patients with chronic kidney disease (CKD) (stage IV-V).

NCT ID: NCT04017806 Recruiting - Clinical trials for Arteriovenous Fistula

Investigating the Role of Luminal Pressure on Arteriovenous Fistula Maturation

Start date: September 19, 2018
Phase:
Study type: Observational

Introduction Arteriovenous fistula (AVF) is the preferred hemodialysis vascular access due to its higher patency and lower infection rate. However, its major weakness is suboptimal maturation rate. Although that substantial risk factors for AVF maturation failure have been disclosed, a modifiable risk factor remains absent. While contemporary theory for AVF maturation failure focuses on disturbed wall shear stress, complicate assumtions and measurement preclude its clinical applicability. In the process of AVF maturation, elevated luminal pressure is required for outward remodeling, however, exccessively high luminal pressure may also be ditremental to AVF maturation, which remains to be defined. This study hypothesize that higher AVF luminal pressure is harmful to its maturation and investigate its potential as a modifiable factor to improve AVF maturation. Methods and analysis This prospective study includes patients receiving surgical creation of native AVF. The exclusion criteria include age <20 years, inability to sign inform consent and failure to create native AVF deu to technical difficulty. Demographic and labboratory profile will be collected before AVF surgery. Vascular sonography will be performed within 1 week of AVF creation to measure the blood flow rates and diameters of AVF and its branched veins. The pressure gredient within AVF will be estimated from blood flow rates by Modified Bernoulli Equation. The primary outcome was spontaneous AVF maturation defined as provision of sufficient blood flow for hemodialysis within 2 months of its creation without any interventional procedures. The secondary outcome is assisted AVF mature, which is defined as AVF maturation within 2 months from its creation, which is aided by any interventional procedure before successful use of AVF. Ethics and dissemination This study has been approved by the ethics committee and Institutional Review Board of Taipei Medical University. Strengths and limitations 1. The strength of the present study is the prospective design that allows complete collection of parameters and outcomes. 2. The predictor of interest for AVF maturation is luminal pressure of AVF. 3. The study assesses hemodynamic parameters of AVF and its branched veins, including diameters, flow rates, and flow volume. 4. The luminal pressure of AVF will be estimated using Modified Bernoulli Equation. 5. The primary outcome of the study is spontaneous AVF maturation.

NCT ID: NCT04015674 Recruiting - Clinical trials for Chronic Kidney Diseases

Effects of Aerobic Exercise on Arteriovenous Fistula

Start date: March 25, 2019
Phase: N/A
Study type: Interventional

Arteriovenous fistula (AVF) is considered the gold standard for safe and effective vascular access during hemodialytic treatment. It is known that systemic aerobic exercise is capable of promoting peripheral vasodilation, however, its effects on AVF are unknown. For this reason, we will evaluate the effects of aerobic exercise on a stationary bicycle over the AVF caliber.

NCT ID: NCT03922438 Recruiting - Clinical trials for Nasoalveolar Fistula (Defect)

Clinical Assessment of Usage of Cleft Margin Flap With Anterior Palatal Closure in Closure of Naso-alveolar Defect.

Start date: October 10, 2018
Phase: N/A
Study type: Interventional

During primary cleft lip repair in patients who were born with cleft lip and palate, usage of cleft margin flap with anterior palatal closure will be done in an attempt to close the Naso-alveolar fistula (defect) that usually occur and remain in those patients post-operatively.

NCT ID: NCT03920306 Recruiting - Clinical trials for Gastrostomy Complications

A Prospective Evaluation of Non-Operative Treatments for Gastrocutaneous Fistulae in Children

GCF
Start date: April 1, 2019
Phase: Phase 4
Study type: Interventional

Gastrostomy tube placement is a common surgery, and involves placing a tube from the child's skin to the inside of their stomach, allowing an alternative route for nutrition and medication to patients who cannot tolerate oral intake. A common complication of gastrostomy tubes is the development of a persistent connection between the stomach and skin after their removal. This is called a gastrocutaneous fistula (GCF). Non-surgical options have shown some success in eliminating the need for surgery to close these fistulae. Their true efficacy is unknown however; this study evaluates a non-surgical intervention bundle in the prevention and treatment of GCFs.

NCT ID: NCT03913910 Recruiting - Perianal Fistula Clinical Trials

Perianal Fistula Treatment With Autologous Adipose Tissue Injection

Start date: February 1, 2019
Phase:
Study type: Observational

The study aims to evaluate the efficacy of the local injection of autologous micro-fragmented adipose tissue obtained with the Lipogems®system in patients with trans-sphincteric fistulas untreatable with fistulotomy.

NCT ID: NCT03913572 Recruiting - Crohn Disease Clinical Trials

Treatment of Perianal Disease Using Adipose-derived Stem Cells

Start date: September 27, 2018
Phase:
Study type: Observational

This study will compare healing and surgical outcomes in patients with chronic perianal disease treated with Adipose-derived Stem Cells (ASCs) to outcomes in patients treated in traditional surgical techniques without ASCs. The study will perform retrospective medical record analysis to clinically characterize patients that have undergone these surgical procedures and compare follow-up data and disease status to determine efficacy of treatment with ASCs compared to similar treatments without the use of ASCs. This will help determine overall efficacy of the treatment as well as determine patient characteristics that may predict treatment success. The study will also prospectively recruit patients with perianal disease that are planning to receive treatment with ASCs, and analyze their outcomes in the same way. Medical record review of outcomes in patients with perianal disease that received treatment with ASCs compared to those that did not will determine efficacy of this procedure.