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Rectal Fistula clinical trials

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NCT ID: NCT04310800 Recruiting - Anal Fistula Clinical Trials

LIFT-plug vs LIFT, a RCT Trial

LIFT 02
Start date: January 1, 2018
Phase: N/A
Study type: Interventional

To validate the effect of Ligation of Intersphincteric Fistula Tract (LIFT) Versus LIFT-plug procedure for Anal Fistula Repair in 7 medical centers

NCT ID: NCT04190862 Recruiting - Anal Fistula Clinical Trials

E-CEL UVEC as an Adjunct Cell Therapy for Treatment of Anal Fistulas

Start date: January 22, 2020
Phase: Phase 1
Study type: Interventional

The purpose of this study is to determine if endothelial cells derived from human umbilical vein are safe for use in conjunction with fistulotomy for the treatment of simple anal fistulas. Endothelial cells are a special kind of cell in the body that line the inside surface of blood vessels. The goal of the study is to evaluate the preliminary safety of human umbilical vein cells in anal fistula healing.

NCT ID: NCT04178707 Recruiting - Anal Fistula Clinical Trials

Anal Fistula and Microdialysis - What is Yet to Learn?

Start date: December 10, 2019
Phase: N/A
Study type: Interventional

Anal Fistula can be a challenging condition to treat. Microdialysis has never before been used to examine the inner environment of anal fistula. This is now going to be performed.

NCT ID: NCT04161469 Recruiting - Anal Fistula Clinical Trials

Laser Closure of Anal Fistula (FiLaC)

Start date: August 1, 2019
Phase: N/A
Study type: Interventional

Laser closure of the perianal fistula is the minimally invasive and low complication rate procedure which is a life-saving way for complex fistulas, preserving anal sphincter injury. Unfortunately, wide range success rate reported before (30-80%), the investigators are searching to reach better rates. Internal closure of the fistula orifice offered by some authors. The investigators are aimed to identify the efficiency of this.

NCT ID: NCT04119700 Recruiting - Anal Fistula Clinical Trials

Fistulectomy and Primary Sphincter rEconstruction vs. endorectaL Advancement Flap in the Treatment of High Anal Fistulas

SELF
Start date: November 4, 2017
Phase: N/A
Study type: Interventional

The optimal method of surgical treatment of complex anorectal fistulas has not been found yet. The aim of this study is to compare two techniques in treatment of high anorectal fistulas. This study purpose to demonstrate that the fistulectomy with dissection from 1/3 to 2/3 of the height of the sphincter complex with primary suturing is technically simpler, equally effective and safe in comparison with muco-muscular endorectal advancement flap.

NCT ID: NCT03913910 Recruiting - Perianal Fistula Clinical Trials

Perianal Fistula Treatment With Autologous Adipose Tissue Injection

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

The study aims to evaluate the efficacy of the local injection of autologous micro-fragmented adipose tissue obtained with the Lipogems®system in patients with trans-sphincteric fistulas untreatable with fistulotomy.

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: 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: NCT03743701 Recruiting - Anal Fistula Clinical Trials

Endorectal Three-dimensional Ultrasound in the Diagnosis of Cryptogenic Fistulas of the Rectum.

Start date: December 30, 2017
Phase: N/A
Study type: Interventional

Prospective comparative parallel ultrasound diagnostic transrectal study in the diagnosis of cryptogenic fistulas of the rectum

NCT ID: NCT03707769 Recruiting - Perianal Fistula Clinical Trials

TIPS Microspheres for Perianal Fistula

Start date: March 15, 2017
Phase: N/A
Study type: Interventional

Phase of Investigation: First-in-human feasibility study Objectives: Primary objective: Demonstration that TIPS microspheres do not compromise the clinical condition or safety of the patient. Secondary objective: To demonstrate that TIPS microspheres facilitate natural healing in the context of perianal fistula. Type of Investigation: First-in-human single site, open label, feasibility study to assess the safety of TIPS microspheres in perianal fistulas and indicative functionality. Investigation design and methods: First-in-human single delivery of a bioabsorbable device to treat perianal fistula. A standard of care internal flap procedure performed to close the internal fistula opening and up to 300 mg of TIPS microspheres will be inserted into each perianal fistula. Participants will be assessed for healing, inflammation, abscess, sepsis, pain and continence by clinical assessments, blood tests, MRI and questionnaires.