Clinical Trials Logo

Fistula clinical trials

View clinical trials related to Fistula.

Filter by:

NCT ID: NCT03828253 Recruiting - ESRD Clinical Trials

Ellipsys Fistula for Hemodialysis Access

Start date: August 27, 2018
Phase:
Study type: Observational [Patient Registry]

To report the outcomes of patients having percutaneous proximal radial artery fistula creation.

NCT ID: NCT03822676 Recruiting - Pancreatic Fistula Clinical Trials

Prophylactic Pancreatic Stent for the Prevention of Post Operative Pancreatic Fistula

Start date: January 22, 2019
Phase: N/A
Study type: Interventional

Postoperative pancreatic fistula (POPF) remains one of the most harmful complications after pancreatic resection. Some studies have indicated that endoscopic pancreatic stenting was effective in the treatment of POPF. However, the results of prospective RCTs for the prophylactic effect of pancreatic stent insertion against POPF were controversial. This single center prospective randomized trial was designed to compare the outcome after segmental pancreatectomy with prophylactic drainage stent versus no stent.

NCT ID: NCT03812731 Completed - Distal Hypospadias Clinical Trials

Incidence of Urethrocutaneous Fistula With and Without Caudal Epidural Block

Start date: February 22, 2019
Phase: N/A
Study type: Interventional

The study is designed to explore any association between the caudal epidural block(CEB) given for perioperative analgesia and the occurrence of urethrocutaneous fistula postoperatively in children undergoing distal hypospadias repair .We also intend to study the duration of penile engorgement due to CEB causing penile oedema which may subsequently play a role in fistula formation. The pilot study will recruit children under 8 years of age diagnosed with distal hypospadias scheduled to undergo Tubularised Incised Plate Urethroplasty, operated by a single paediatric surgeon. General anaesthesia will be induced with sevoflurane in oxygen nitrous oxide mixture supplemented by fentanyl citrate and atracurium besylate in all children. LMA Pro SealTMof appropriate size will be inserted. Children in group I will then be given caudal epidural block (CEB) as per our practice protocol. Children in group II will be given additional intravenous fentanyl citrate. All children will be followed postoperatively till 3 months to evaluate incidence of urethtocutaneous fistula. The prospective study attempts to eliminate previously reported confounding factors.

NCT ID: NCT03803917 Completed - Crohn Disease Clinical Trials

Adipose Tissue in Crohn´s Disease Fistulas

Start date: March 1, 2015
Phase: N/A
Study type: Interventional

Present study investigated the efficacy of injection of freshly collected autologous adipose tissue into perianal fistulas in patients with Crohn's disease. Adipose tissue collected by liposuction was injected into the perianal fistulas. Primary objective was complete clinical healing six months after treatment. Secondary objectives were reduced or ceased fistula secretion and complications to the treatment.

NCT ID: NCT03800940 Completed - Pancreatic Fistula Clinical Trials

Trans-drain Occlusion for Postoperative Pancreatic Fistula- A Double Blind Randomized Clinical Trial

Start date: January 11, 2019
Phase: N/A
Study type: Interventional

This is a multicenter, investigator initiated, prospective, superiority, parallel-group, randomized, double-blinded trial that aims to compare the efficacy and safety of trans-drain occlusion followed by gradual withdrawal of drain versus gradual withdrawal of drain alone for postoperative pancreatic fistula (POPF) that persists for longer than 21 days.

NCT ID: NCT03792360 Withdrawn - Clinical trials for Tracheoesophageal Fistula

Adipose Derived SVF for Aero-digestive & Enterocutaneous Fistulae

Start date: February 2021
Phase: Phase 1
Study type: Interventional

Determine safety and feasibility of using institutionally prepared autologous, uncultured SVF on patients with aerodigestive and enterocutaneous fistulae secondary to malignancy, trauma or surgery.

NCT ID: NCT03780998 Not yet recruiting - Hemorrhoids Clinical Trials

Effects of Sodium Pentaborat Based Gel on Perianal Benign Diseases

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

New produced and patented sodium pantaborat based gel will be use for treatment of benign perianal diseases (hemooroidal disease, anal fissura anda perianal fistula)

NCT ID: NCT03776825 Recruiting - Crohn Disease Clinical Trials

Permacol Paste in Perianal Crohn's Disease

UPpCro
Start date: February 7, 2019
Phase:
Study type: Observational

The purpose of this study is to collect data about the efficacy of Permacol Paste treatment in perianal Crohn's Disease.

NCT ID: NCT03773237 Active, not recruiting - Crohn Disease Clinical Trials

Intralipid Versus SMOFlipid in HPN Patients

Start date: December 31, 2018
Phase: N/A
Study type: Interventional

This study will randomize all patients who are new to the Mayo Clinic HPN team to either standard lipid emulsion (Intralipid) or SMOFLipid.

NCT ID: NCT03772873 Active, not recruiting - Pilonidal Disease Clinical Trials

MIPE for Pilonidal Disease

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

Pilonidal disease often presents as a chronic, relapsing condition. A variety of procedures are used in the management of pilonidal disease, with varying degrees of morbidity, disease-free interval, and long-term success. In patients with new-onset or recurrent pilonidal disease, the investigators aim to address how minimally invasive trephine excision compares to other surgical procedures in terms of short- and long-term clinical outcomes and patient satisfaction. In the absence of a gold standard surgical procedure, surgeon preference will help dictate the management of pilonidal disease. For many surgeons, this means a variation on open excision for pilonidal disease failing conservative management. However, outcomes for minimally invasive pilonidal excision (MIPE) as initially described by Gips and forthcoming Lipskar et al., are likely to alter management of the disease (Gips, 2008). The investigators wish to assess patient and surgeon satisfaction with MIPE, and short-term outcomes.