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Fistula clinical trials

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NCT ID: NCT01602081 Completed - Anal Fistula Clinical Trials

Ligation of the Intersphincteric Fistula Tract (LIFT) + Biodesign for Anal Fistula

LIFT+Graft
Start date: January 2013
Phase: N/A
Study type: Observational

The LIFT+Biodesign® study is a post-market observational study to evaluate the rate of fistula closure in patients with persistent trans-sphincteric anal fistula who receive the Biodesign® Tissue graft as part of their LIFT procedure.

NCT ID: NCT01561066 Completed - Clinical trials for Intra-abdominal Infection

Autologous Fibrin Glues for Fistulas Closure

Start date: January 2008
Phase: Phase 1
Study type: Interventional

Adjuvant use of fibrin glue in the fistula tract may promote healing in low-output enterocutaneous fistulas. However, there are only few studies that report autologous glue application in a larger patient group or clinical-controlled studies in this setting. The aim of this study was to investigate the efficacy and safety of autologous platelet-rich fibrin glue (PRFG) in the treatment of low-output digestive fistulas and compare them with conservative management without the use of adjuvant application of FG into the fistulous tract.

NCT ID: NCT01550406 Completed - Pancreatic Fistula Clinical Trials

Use of Polyethylene Glycolic Acid or Tachocomb to Prevent Pancreatic Fistula Following Distal Pancreatectomy

Start date: November 2011
Phase: Phase 4
Study type: Interventional

To date, there has been many methods suggested to reduce pancreatic fistula. But there are no evidence of superiority to the other methods. This study is a multicenter prospective randomized phase III study of use of Tachocomb or Polyethylene Glycolic Acid (PGA) to prevent of pancreatic fistula after distal pancreatectomy.

NCT ID: NCT01544907 Completed - Clinical trials for Stenosis of Arteriovenous Dialysis Fistula

Prospective Randomized Trial Comparing DEB Versus Conventional PTA for the Treatment of Hemodialysis AVF or AVG Stenoses

DEBAPTA
Start date: January 2012
Phase: N/A
Study type: Interventional

A prospective randomized trial comparing the efficacy of drug eluting balloon angioplasty versus conventional percutaneous transluminal angioplasty balloon for the treatment of hemodialysis arterio-venous fistula or arterio-venous graft stenoses in reducing late luminal loss and restenosis rates, while prolonging primary and secondary patencies.

NCT ID: NCT01536548 Completed - Clinical trials for Chronic Kidney Disease

Indicating Direction and Angle for Cannulating of AV-fistula in Hemodialysis Patients

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

Arteriovenous fistula is the preferred access for hemodialysis, and cannulation using a "button-hole" technique is increasingly recommended. By using the same two sites for cannulation there are reports of less risk of complications and less pain for the patient. However, button-hole cannulation can be difficult for the dialysis nurse, and failing cannulations can damage the AV fistula and increase patient discomfort. The investigators therefore will test whether a simple marking on the skin of the direction and angle of cannulation used in each specific patient could improve the probability of a successful and painfree cannulation.

NCT ID: NCT01471041 Completed - Clinical trials for End Stage Renal Disease

Safety and Efficacy Study of the Venous Window Needle Guide to Access Arteriovenous (AV)Fistulae

SAVE
Start date: December 2011
Phase: Phase 2/Phase 3
Study type: Interventional

The SAVE Study will evaluate the safety and efficacy of the Venous Window Needle Guide in achieving access of a deep, un-cannulatable arteriovenous fistula to complete hemodialysis as prescribed.

NCT ID: NCT01469442 Completed - Hepatectomy Clinical Trials

Postoperative Biliary Fistula Prevention After Hepatectomy

Start date: May 2009
Phase: N/A
Study type: Interventional

Aim : Effect of external biliary duct stent after hepatectomy on the occurence of postoperative biliary fistula. Methods : French prospective multicenter randomized trial. Population study: Adult patients who underwent hepatectomy (> 2 segments) on non-cirrhotic liver. Hypothesis: decreased postoperative biliary fistula from 15% to 5% with the presence of a external biliary duct stent. With this hypothesis, the number of patients required to be equal to 152 per group for a total of 304 patients. Outcome measure: Primary : Postoperative biliary complications (biliary fistula, biloma, biliary peritonitis) Secondary : All morbidity, mortality, additional manoeuvres to treat biliary fistula, during of hospital stay and biliary fistula. Follow up: A follow-up of patients 3 months after surgery for all patients. The planned total duration of the study is 3 years and 3 months.

NCT ID: NCT01467245 Completed - Clinical trials for Congenital Diaphragmatic Hernia

Open or Keyhole Surgery Through the Chest for Newborn Babies: Effect on Blood Gases

CO2
Start date: August 2009
Phase: N/A
Study type: Interventional

This is a pilot randomised controlled trial comparing open versus thoracoscopic surgery for repair of oesophageal atresia with tracheo-oesophageal fistula or congenital diaphragmatic hernia in neonates. Thoracoscopic surgery involves insufflation of carbon dioxide into the thoracic cavity and may therefore cause hypercapnia and acidosis.

NCT ID: NCT01462747 Completed - Perianal Fistulas Clinical Trials

Efficacy and Safety Study of a Medical Device (KULIST)to Treat Perianal Fistulas

Start date: December 2011
Phase: Phase 2
Study type: Interventional

The aim of this study is to evaluate the effects of rectally administered activated carbon (medical device KULIST) in chronic, uncomplicated, perianal fistulas.

NCT ID: NCT01440699 Completed - Crohn Clinical Trials

Study of Allogenic Adipose-derived Stem Cells in Crohn's Fistula

ALLO-ASC
Start date: September 2011
Phase: Phase 1
Study type: Interventional

Adipose-derived stem cells have properties of differentiation to various types of cells, immunomodulatory effects. adipose-derived stem cells (ASCs) show also low immunogenicity. Anterogen has developed ANTG-ASC(Autologous ASC) which has shown good efficacy and safety in Phase I and II study on the patients with Crohn's fistula. However, Crohn's patients are sometimes not fat enough to extract fat tissue for culturing ASCs. Therefore the investigators have planned to study allogenic ASCs for safety and efficacy in patients with Crohn's fistula.