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Fistula clinical trials

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NCT ID: NCT00923338 Completed - Clinical trials for Vesico-vaginal Fistula

Clinical Evaluation of the Surgisis Biodesign Vesico-Vaginal Fistula Plug

VVP
Start date: September 2009
Phase: N/A
Study type: Interventional

This clinical trial will study the safety and effectiveness of the Biodesign Vesico-vaginal fistula plug in the treatment of vesico-vaginal fistulas resulting from childbirth trauma.

NCT ID: NCT00911014 Completed - Clinical trials for Delivery of Healthcare

Access to Healthcare, Patient Comprehension and Future Plans of Women Undergoing Surgery for a Vesicovaginal Fistula in Niamey, Niger

Start date: September 2005
Phase: N/A
Study type: Observational

Evaluate access to healthcare, comprehension of pre-operative counseling and post-operative goals of women treated for vesicovaginal fistula in Niger through use of a questionnaire.

NCT ID: NCT00836862 Completed - Clinical trials for Kidney Failure, Chronic

Arteriovenous Fistula Tissue Bank for Pre- and Post-Fistula Placement Specimens

Start date: February 1, 2009
Phase:
Study type: Observational

This project will bank sera, DNA and vascular specimens from patients undergoing arteriovenous fistula creation and revision.

NCT ID: NCT00737620 Completed - Clinical trials for Hemodialysis Fistula Thrombosis

Evaluation of Heparin Bonded Vascular Graft Versus Standard Graft in Prosthetic Arteriovenous Access for Hemodialysis

Start date: March 2008
Phase: Phase 4
Study type: Interventional

The majority of bridge graft fistula with polytetrafluoroethylene (PTFE) for hemodialysis access will develop stenosis at the venous anastomosis and eventually will fail. Aspirin have been used for many years as a prophylactic drug therapy to prevent thrombosis but good clinical evidence for its benefit is lacking. Many drugs have been used to reduce intimal hyperplasia in animal models. Until recently there has been little success in clinical trials of anti-inflammatory, antiproliferative, antiplatelet, antithrombotic or calcium channel blocking drugs. Recently a major breakthrough was done by GORE when introducing the new heparin bonded PTFE graft by covalent attachment. This trial is planed to assess and compare between the GORE-TEX® PROPATEN vascular graft versus unmodified ePTFE grafts the patency and complication.

NCT ID: NCT00736983 Completed - Clinical trials for Crohn's Disease With Perianal Fistulas

Adalimumab in Combination With Ciprofloxacin/Placebo Treatment of Perianal Fistulas in Crohn's

Adafi
Start date: September 2008
Phase: Phase 3
Study type: Interventional

To assess whether a combination of ciprofloxacin and adalimumab is more effective than adalimumab alone for the treatment of perianal fistulas in Crohn's disease

NCT ID: NCT00729313 Completed - Digestive Fistulae Clinical Trials

Efficacy and Safety of Lanreotide Versus Placebo for Treatment of Patients With Digestive Fistulae

Start date: April 2000
Phase: Phase 3
Study type: Interventional

The purpose of the protocol, is to determine whether lanreotide 30 mg is effective in the treatment of patients with digestive fistulae.

NCT ID: NCT00703131 Completed - Anal Fistula Clinical Trials

Surgisis Anal Fistula Plug Study: An Experience in Saudi Arabia

SurgiSIS AFP
Start date: April 2009
Phase: N/A
Study type: Observational

The Surgisis Anal Fistula Plug study is a clinical trial conducted in Saudi Arabia to study the safety and effectiveness of the Surgisis AFP Plug in the treatment of chronic anal fistulas.

NCT ID: NCT00545441 Completed - Anal Fistula Clinical Trials

A Randomized Clinical Trial Comparing Surgisis AFP to Advancement Flap for the Repair of Anal Fistulas

Surgisis® AFP
Start date: June 2008
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether the Surgisis anal fistula plug is just as effective in healing anal fistulas as compared to the advancement flap procedure.

NCT ID: NCT00544492 Completed - Dialysis Clinical Trials

Study of Pain, Anxiety and Complications Related to Cannulation of Arteriovenous (AV) Fistula in Chronic Hemodialysis Patients

Start date: October 2007
Phase: Phase 4
Study type: Interventional

A. Pain and other disadvantages of AV fistula cannulation can be limited by using the so-called buttonhole technique. B. Till present in our center catheters with cylindrical points are used for cannulation of AV fistulas with the rope ladder technique. One can hypothesize that a catheter with a bevel point might have some advantages such as a larger entrance area and less traumatic cannulation. The latter may influence pain sensation of the patients. The above background information gives rise to the following investigational questions: A. Buttonhole vs rope ladder technique 1. Is pain sensation different when using buttonhole cannulation as compared to rope ladder cannulation technique? Hypothesis: AV fistula cannulation by buttonhole technique causes less pain than cannulation by rope ladder technique. 2. Is the level of anxiety different when using buttonhole cannulation as compared to rope ladder cannulation technique? Hypothesis: AV fistula cannulation by buttonhole technique causes less anxiety than cannulation by rope ladder technique. 3. Is bleeding time different when using buttonhole cannulation as compared to rope ladder cannulation technique? Hypothesis: Bleeding time is shorter when using buttonhole technique versus rope ladder technique. 4. Is the number and severity of complications related to AV fistula cannulation different between buttonhole and rope ladder technique? Hypothesis: When using the buttonhole technique for AV fistula cannulation the number and severity of complications is less than when using the rope ladder technique. B. Rope ladder technique using catheters with cylindrical vs. bevel point 5. Is pain sensation different when using rope ladder cannulation catheters with cylindrical as compared to bevel point? Hypothesis: AV fistula cannulation using bevel point catheters causes less pain than cannulation using cylindrical point catheters.

NCT ID: NCT00500968 Completed - Pancreas Cancer Clinical Trials

Study Assessing the Effect of Transpapillary Pancreas Duct Stent in Resection of the Pancreatic Tail

Start date: November 2006
Phase: N/A
Study type: Interventional

Randomized study assessing the effect of transpapillary pancreas duct stent in resection of the pancreatic tail.