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Fistula clinical trials

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NCT ID: NCT04634916 Recruiting - Clinical trials for End-stage Renal Disease

Post-market Surveillance Study of the BD® WavelinQ™ EndoAVF System

CONNECT-AV
Start date: March 26, 2021
Phase: N/A
Study type: Interventional

A prospective, single-arm, multi-center post-market surveillance study of the BD® WavelinQ™ EndoAVF System for the Creation of Arteriovenous (AV) Fistula in Patients Requiring Dialysis.

NCT ID: NCT04616911 Recruiting - Anal Fistula Clinical Trials

Rerouting Seton Versus LIFT for Complex Anal Fistula

Start date: November 1, 2020
Phase: N/A
Study type: Interventional

This study aims to compare the efficacy of two surgical techniques in treatment of complex anal fistulas. The first technique involves rerouting of the fistula tract with placement of a vessel loop seton around the internal anal sphincter, sparing the external sphincter whereas the second technique entails ligation of inter-sphincteric fistulous tract (LIFT). The main objectives of the study are to assess the success rate, time to healing, change in quality of life, and complications of each procedure including fecal incontinence.

NCT ID: NCT04612465 Recruiting - Crohn's Fistula Clinical Trials

Clinical Study to Evaluate Efficacy and Safety of ASC and Fibringlue or Fibringlue in Patients With Crohn's Fistula

Start date: January 9, 2020
Phase: Phase 3
Study type: Interventional

This is a phase III study to evaluate the efficacy and safety of ASC(Autologous Adipose-derived Stem Cells) and Fibringlue or Fibringlue in Patients With Crohn's Fistula.

NCT ID: NCT04577859 Recruiting - Complication Clinical Trials

Oesophageal Protection Study: A Multicentre Study.

IMPACT II
Start date: March 10, 2022
Phase: N/A
Study type: Interventional

Atrial fibrillation (AF) is a common debilitating heart rhythm condition that can cause heart failure and negatively impact a patient's outlook in terms of symptoms and disability. It is an irregular fast heart rhythm disorder coming from the top chamber of the heart (left atrium). Catheter ablation treatment has been shown to be effective in controlling or eliminating AF and its associated symptoms. This is now a common and effective treatment option for patients suffering with AF. During ablation, thermal energy is applied in the top chamber of the heart (the left atrium) to abolish abnormal electrical signals that cause AF. It is generally a safe procedure, but one potential risk associated with this procedure is damage to the oesophagus caused by thermal energy being transmitted to the oesophagus from the heart. The oesophagus sits just behind the heart chamber where ablation work is performed, about 5mm away, so it is vulnerable to damage. Although the risk of severe oesophageal damage is low, if it occurs it can be serious as the patient may become very ill as a result. In a recent study, it was shown that a more advanced type of oesophageal probe that cools the oesophagus during ablation is better at protecting the oesophagus from ablation-related injury compared to the standard care probe currently used. As it was a single-centre study, more evidence is required before knowing if this type of probe is more effective in protecting the oesophagus. The purpose is to run a multi-centre randomized study to compare the safety of AF ablation when there is protection by the oesophageal cooling probe versus the standard of care oesophageal temperature monitoring probe. This means that there is a 50:50 chance of the new cooling probe being used during AF ablation for participants.

NCT ID: NCT04577456 Recruiting - Ileostomy - Stoma Clinical Trials

Chyme Reinfusion for Type 2 Intestinal Failure

REINFUSE
Start date: October 15, 2022
Phase: N/A
Study type: Interventional

This project aims to introduce and evaluate a novel assistive prosthetic system that helps prevent and treat nutrient and fluid loss from enterocutaneous fistulas. The device system functions simply to return the output from a fistula back into the distal limb of the intestine.

NCT ID: NCT04571541 Recruiting - Clinical trials for Esophageal Perforation

Endoscopic Management of Esophageal Wall Defects

Start date: July 1, 2014
Phase:
Study type: Observational

The study aim at comparing outcomes from the implementation of various endoscopic closure techniques including stenting and suturing on the healing and resolution of esophageal wall defects.

NCT ID: NCT04543539 Recruiting - Clinical trials for Arteriovenous Fistula

IN.PACT™ AV Access Post-Approval Study (PAS002)

Start date: November 13, 2020
Phase:
Study type: Observational [Patient Registry]

Long-term safety will be summarized

NCT ID: NCT04519697 Recruiting - Crohn Disease Clinical Trials

Mesenchymal Stem Cells for the Treatment of Rectovaginal Fistulas in Participants With Crohn's Disease

RVF
Start date: October 28, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Approximately 10% of all female Crohn's patients have a rectovaginal fistula. Rectovaginal fistulas cause air, stool, and/or drainage per vagina and may be associated with pain, recurrent urinary tract infections and diminished quality of life. Conventional therapy includes immunosuppressive medications used to treat Crohn's disease and various surgical interventions. However, all have limited ability to heal these fistulas. The purpose of this study is to determine the safety and efficacy of using allogeneic bone marrow derived mesenchymal stem cells (MSCs) to treat people with rectovaginal fistulas in the setting of Crohn's disease.

NCT ID: NCT04519684 Recruiting - Crohn Disease Clinical Trials

Study of Mesenchymal Stem Cells for the Treatment of Ileal Pouch Fistula's in Participants With Crohn's Disease

IPAAF
Start date: October 28, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

Restorative proctocolectomy with ileal pouch anal anastomosis (IPAA) is the procedure of choice for patients with ulcerative colitis, familial adenomatous polyposis, and select patients with Crohn's disease due to overall low patient morbidity and good quality of life. However, some patients can develop Crohn's disease of the pouch, a clinical diagnosis of Crohn's disease following IPAA. One of the manifestations of Crohn's disease of the pouch includes a fistula from the pouch that travels to the vagina or perianal area. These fistulas can be quite difficult to manage with medications and local surgical intervention, and, on occasion result in a reconstruction pouch but more often require a pouch excision with permanent end ileostomy. The purpose of this study is to evaluate the safety and efficacy of using allogeneic bone marrow derived mesenchymal stem cells to treat people who have a peri-pouch fistula related to a clinical diagnosis of Crohn's disease of the pouch.

NCT ID: NCT04519671 Recruiting - Crohn Disease Clinical Trials

Mesenchymal Stem Cells for the Treatment of Perianal Fistulizing Crohn's Disease

PFCD
Start date: November 19, 2020
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of using adult allogeneic bone marrow derived mesenchymal stem cells (MSCs), to treat people for medically refractory perianal fistulizing Crohn's disease.