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Fistula clinical trials

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NCT ID: NCT03264430 Active, not recruiting - Hemorrhoids Clinical Trials

Adding Ketamine to Low Dose Bupivacaine in Saddle Block for Perianal Surgery

Start date: January 1, 2017
Phase: Early Phase 1
Study type: Interventional

Evaluation of the anesthetic quality and analgesic efficacy of adding ketamine to intrathecal bupivavaine in selective saddle block for perianal surgery.

NCT ID: NCT03236922 Active, not recruiting - Clinical trials for Vesicovaginal Fistula

Autologous Slings With Vesico-Vaginal Fistula Repair

Start date: June 2016
Phase: N/A
Study type: Interventional

It is clear from multiple accounts in the literature that patients with a vesico-vaginal fistula (VVF) involving the bladder neck and/or proximal urethra have a high likelihood of residual incontinence. Performing subsequent surgeries after the initial VVF repair risks additional complications. Therefore, placement of an autologous sling at the time of initial VVF repair would not only assist in covering the fistula, but would also imitate the physiologic support that would theoretically improve urethral function. A rectus fascia sling would most naturally provide this support and warrants testing against the success of the PC sling. Using the Goh scoring criteria, Goh class 3 and 4 VVF's are the type most involving the urethra. Therefore, this group of patients is the target population for this study. As there is currently no standard of care for repairing large urethral defects, this procedural technique combined with otherwise standardized fistula repair would not introduce any foreseeable harm to patients.

NCT ID: NCT03183245 Active, not recruiting - Clinical trials for End Stage Renal Disease

Comparison of the Human Acellular Vessel (HAV) With Fistulas as Conduits for Hemodialysis

Start date: September 29, 2017
Phase: Phase 3
Study type: Interventional

The main purpose of this study is to compare the Human Acellular Vessel (HAV) with arteriovenous fistula (AVF) when used for hemodialysis access

NCT ID: NCT02861950 Active, not recruiting - Hypospadias Clinical Trials

Does Caudal Block Increase the Incidence of Urethrocutaneous Fistula Formation Following Hypospadias Repair in Infants?

Start date: May 24, 2017
Phase: Phase 4
Study type: Interventional

This is a prospective randomized multi-center non-inferiority trial conducted through the Pediatric Regional Anesthesia Network study sites to determine if caudal block increases the incidence of urethrocutaneous fistula following distal or mid shaft hypospadias repair compared with penile nerve block.

NCT ID: NCT02808208 Active, not recruiting - Clinical trials for Vascular Access Complication

Autologous Adipose Derived Mesenchymal Stem Cells (AMSC) in Reducing Hemodialysis Arteriovenous Fistula Failure

Start date: June 7, 2017
Phase: Phase 1/Phase 2
Study type: Interventional

The aim of this phase 1 study is to determine the role of autologous adipose derived mesenchymal stem cells in the reduction of hemodialysis arteriovenous fistula failure when applied during the time of surgical creation.

NCT ID: NCT02775227 Active, not recruiting - Clinical trials for Pancreatic Neoplasms

HYPAR Trial - Hydrocortisone vs. Pasireotide in Reducing Pancreatic Surgery Complications

HYPAR
Start date: May 2016
Phase: Phase 4
Study type: Interventional

Pancreatic resections carry a high risk for complications, especially pancreatic fistula. Both hydrocortisone and pasireotide have been shown to be effective in reducing complications in earlier RCTs. The aim of this study is to compare the effectiveness and safety of these two drugs in preventing complications of pancreatic surgery.

NCT ID: NCT01931371 Active, not recruiting - Anal Fistula Clinical Trials

Anal Fistula Plug Versus Endorectal Advancement Flap

AFPERAF
Start date: May 2007
Phase: N/A
Study type: Interventional

The purpose of this study is to determine whether anal fistula plug or endorectal advancement flap is more successful in the treatment of anal fistulas and compared both procedures with regards to cost.

NCT ID: NCT01693263 Active, not recruiting - Dialysis Clinical Trials

Outcome of BCF Access in Hemodialysis Patients

BCF
Start date: October 2011
Phase:
Study type: Observational

Dialysis access, which is the connection that allows blood to flow in and out of the body during dialysis sessions, is important to remove wastes and excess fluid for patients with end stage renal disease (ESRD). One method used to access the vein and artery for dialysis is called a brachiocephalic fistula. Patients are being asked to participate in this study because they have endstage renal disease, and their doctor has recommended that they will have brachiocephalic fistula placed for their dialysis access. A common problem seen in patients with a brachiocephalic fistula (BCF) is cephalic arch stenosis (CAS). CAS is a narrowing in the central vein (located in the upper chest). CAS causes problems with the opening of the veins and arteries needed for dialysis. Once someone suffers CAS they may need several radiology procedures as well as surgery to help correct the problem. The BCF may fail once CAS develops. The purpose of the research study is to gather information about the BCF and what is happening inside the vein. The researchers hope to find out what may be the cause of CAS.

NCT ID: NCT00517296 Active, not recruiting - Crohn Disease Clinical Trials

Endoscopic Ultrasound (EUS) Guided Treatment With Humira for Crohn's Perianal Fistulas

Start date: January 2008
Phase: N/A
Study type: Interventional

This study is to assess whether utilizing endoscopic ultrasound(EUS) to guide treatment can improve durable fistula healing in patients with Crohn's perianal fistulas and to get preliminary information regarding the effectiveness of Adalimumab for Crohn's perianal fistulas.

NCT ID: NCT00115466 Active, not recruiting - Anal Fistula Clinical Trials

Autologous Stem Cells Derived From Lipoaspirates for the Non-Surgical Treatment of Complex Perianal Fistula

Start date: October 2004
Phase: Phase 2
Study type: Interventional

This comparative, multicentre, randomised clinical trial is designed with two parallel groups that will follow a treatment either with an autologous implant of ASCs (Adipose Derived Stem Cells) and fibrin glue (tissue adhesive material) or with fibrin glue alone for the non-surgical treatment of complex perianal fistula.