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Fistula clinical trials

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NCT ID: NCT03904212 Recruiting - Crohn Disease Clinical Trials

Adipose Tissue Injection in Perianal Fistulas in Crohn´s Disease

Start date: March 27, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

This randomized and placebo controlled study investigates the efficacy of injections with freshly harvested autologous adipose tissue in CD patients with complex perianal fistulas refractory to standard surgical and/or medical treatment. 140 CD patients will be included and randomized to either treatment with freshly harvested autologous adipose tissue or placebo (saline). Primary outcome measures are clinical healing 6 months after treatment evaluated by clinical examination and pelvic MRI.

NCT ID: NCT03890523 Recruiting - Airway Disease Clinical Trials

Airway Stent Modified With 3D Printing for Gastro-respiratory Fistula Involving Carina and Distal Bronchi

Start date: March 1, 2017
Phase: N/A
Study type: Interventional

In this study, the investigators used the covered metallic segmented airway stent modified with 3D printing to treat gastro-respiratory fistula involving carina and distal bronchi and aimed to determine the feasibility, efficacy and safety of this technique.

NCT ID: NCT03886116 Recruiting - Clinical trials for End Stage Renal Disease

Effect of Pre-operative Forearm Exercises on Arterial Venous Fistula Maturation and Blood Flow

Start date: November 28, 2018
Phase: N/A
Study type: Interventional

This study will investigate the effect of pre-operative exercise on hemodynamics in the fistula artery and vein, Pre and Post Arteriovenous Fistula Formation as well as the suitability of Cannulation of Arteriovenous Fistula at 12 weeks Post Surgery. This is a randomised control study with 20 patients each in the Control arm (Group A) or the Exercise arm (Group B). The subjects will be randomised into 1:1 into one of the two groups. The patients will have an ultrasound doppler vein mapping done prior surgery and the necessary follow up visits.

NCT ID: NCT03880773 Recruiting - Pancreatic Fistula Clinical Trials

Comparison Between Two Methods of Pancreatic Transection in Distal Pancreatectomy

TRUDY
Start date: July 1, 2018
Phase: N/A
Study type: Interventional

Several systematic reviews have investigated the management of the pancreatic stump in order to reduce the postoperative pancreatic fistula (POPF) rate after distal pancreatectomy (DP). The appropriate closure technique of the pancreatic stump is still debated. There is no published experience about the comparison of the Endo GIA Reinforced Reload with Tri-Staple Technology (TS) versus Harmonic Focus (US) after distal pancreatectomy (DP) regarding the reduction of POPF. The investigators want to compare the incidence of clinically-relevant POPF (CR-POPF) after DP, depending upon the transection technique (TS versus US). This is a randomized controlled, multicenter, patient-blinded, superiority trial. This protocol was designed according to the SPIRIT guidelines. Two groups of 76 patients (152 in total) with an indication for elective minimally invasive or open DP for a lesion of the body-tail of the pancreas. The two techniques analyzed are Endo GIA Reinforced Reload with Tri-Staple Technology (TS) and Harmonic Focus (US) as control. The primary endpoint is to evaluate the incidence of CR-POPF rate after DP. Secondary endpoints are intraoperative outcomes (blood loss, operative time and conversion of the minimally invasive procedure), postoperative outcomes (complications rate; hospitalization parameters to 90 days; mortality) and treatment costs.

NCT ID: NCT03865823 Recruiting - Anal Fistula Clinical Trials

Evaluation of the Recovery Rate and Postoperative Incontinence of Surgical Fistulas in a Cohort of a Reference Centre

PROFIL
Start date: March 1, 2019
Phase:
Study type: Observational

Fistula is a pathology that can be complex and lead to treatment difficulties for the proctologist. The proctologist's objective is to treat the infection (anal fistula and abscess) with the minimum impact on anal continence. Drainage of the fistula pathway(s) and removal of infected tissue during initial surgery are essential. The treatment of upper trans-sphincterial fistulas, i. e. those that span more than half the height of the anal sphincter, poses risks to anal continence. It sometimes requires several times of surgical treatment. The study aim to investigate the fate of all patients treated for anal fistula in an expert team, in terms of impact on healing and anal continence and according to the type of anal fistula, the co-morbidity, the surgical techniques used and the bacterial flora responsible.

NCT ID: NCT03853070 Recruiting - Aneurysm Clinical Trials

Post Market Clinical Follow-Up for ED Coil / Electro-detach Generator v4

Start date: December 11, 2018
Phase:
Study type: Observational

This is a multicenter post-marketing clinical follow-up study to collect safety and performance data in a prospective cohort of patients who will have undergone coil embolization using the ED Coil and ED Detach Generator v4.

NCT ID: NCT03832959 Recruiting - Atrial Fibrillation Clinical Trials

Esophageal Damage Protection During Pulmonary Vein Ablation. Pilot Study.

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

Catheter ablation of atrial fibrillation with electrical isolation of the pulmonary veins in the left atrium carries risk of esophagus thermal lesion. EnsoETM is a device . This study evaluates the benefit of using the EnsoETM, a device device for esophageal temperature adjustments, during catheter ablation of atrial fibrillation. Half of participants will undergo esophageal temperature adjustment during pulmonary vein catheter ablation, while the other half will undergo catheter ablation with no esophageal temperature adjustment.

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: 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.