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Rectal Fistula clinical trials

View clinical trials related to Rectal Fistula.

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NCT ID: NCT01803347 Completed - Anal Fistula Clinical Trials

Clinical Trial to Evaluate the Efficacy and Safety of Stem Cells

FISPAC
Start date: February 2013
Phase: Phase 3
Study type: Interventional

Efficacy of treatment of perianal fistula with mesenchymal stem cells and surgery

NCT ID: NCT01793168 Recruiting - Clinical trials for Retinitis Pigmentosa

Rare Disease Patient Registry & Natural History Study - Coordination of Rare Diseases at Sanford

CoRDS
Start date: July 2010
Phase:
Study type: Observational [Patient Registry]

CoRDS, or the Coordination of Rare Diseases at Sanford, is based at Sanford Research in Sioux Falls, South Dakota. It provides researchers with a centralized, international patient registry for all rare diseases. This program allows patients and researchers to connect as easily as possible to help advance treatments and cures for rare diseases. The CoRDS team works with patient advocacy groups, individuals and researchers to help in the advancement of research in over 7,000 rare diseases. The registry is free for patients to enroll and researchers to access. Visit sanfordresearch.org/CoRDS to enroll.

NCT ID: NCT01624350 Completed - Anorectal Fistulas Clinical Trials

A Prospective, Multi-center, Observational Study of the Use of Permacolâ„¢ Collagen Paste to Treat Anorectal Fistulas

Start date: September 2012
Phase: N/A
Study type: Observational

This will be a prospective, multi-center, post-market, single arm observational study to collect clinical outcome data on the use of Permacolâ„¢ Collagen Paste in the treatment of anorectal fistulas. The subjects will have baseline and day of surgery visits performed, and then subjects will return to the investigator for evaluation of defect and safety related morbidities at follow up visits scheduled at 1 month, 3 months, 6 months and 12 months post-surgery.

NCT ID: NCT01615302 Recruiting - Rectal Fistula Clinical Trials

Is the Use of Blood Platelets Effective in the Treatment of Difficult Fistulas Related to the Anal Sphincter?

Start date: March 2012
Phase: N/A
Study type: Interventional

Rationale: Closure of the internal opening is the most accepted standard procedure in the treatment of peri-anal fistulas. The mucosal advancement flap is considered as golden standard. In one out of the three patients mucosal flap repair fails. Possible causal factors are incomplete clearance of pus and debris, incomplete closure of the internal opening, inappropriate host response in patients with risk factors like smoking or diabetes. Platelet derived growth factors may facilitate closure of the internal opening, especially in patients with impaired wound healing. Objective: The use of autologous platelet rich plasma (PRP) as an adjunct to the staged mucosal advancement flap to achieve a better closure rate of complex peri-anal fistula's. Study design: Randomized, multicenter trial. Study population: Patients with complex cryptoglandular peri-anal fistula's. Intervention: Injection of PRP in the curretted fistula track under the mucosal flap. Main study parameters/endpoints: - Recurrence rate - Post-operative pain - Continence - Quality of life. Nature and extent of the burden and risks associated with participation, group relatedness: Because autologous blood is used, no extra risk are expected.

NCT ID: NCT01612195 Completed - Clinical trials for Complex Anal Fistula

Success Rate, Continence, and Quality of Life With a Bioprosthetic Plug for Treating Complex Anal Fistula

Start date: January 2007
Phase: Phase 2
Study type: Interventional

Anal abscess-fistula disease is of common occurrence and has a significant impact on the quality of life of affected individuals. The course of abscess-fistula disease as well as its treatment modalities may affect anal continence. The present cohort study investigates the results of anal fistula plug surgery. In particular, this study focus on the impact of anal fistula plug surgery on fistula healing, quality of life, and anal continence. Fifty patients will be included and followed up at 6 weeks and 6 months after surgery in the clinic of participating surgeons.

NCT ID: NCT01602081 Completed - Anal Fistula Clinical Trials

Ligation of the Intersphincteric Fistula Tract (LIFT) + Biodesign for Anal Fistula

LIFT+Graft
Start date: January 2013
Phase: N/A
Study type: Observational

The LIFT+Biodesign® study is a post-market observational study to evaluate the rate of fistula closure in patients with persistent trans-sphincteric anal fistula who receive the Biodesign® Tissue graft as part of their LIFT procedure.

NCT ID: NCT01586715 Recruiting - Clinical trials for Extremely Complex Perianal Fistulae

Stem Cells Treatment for Extremely Complex Fistulae (HULPCIR)

Start date: March 2012
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the practicability of the autologous e-ASC (Autologous Stem Cells) for the treatment of extremely complex and treatment resistant perianal fistulae.

NCT ID: NCT01584752 Terminated - Surgery Clinical Trials

Gore-BioA Fistula Plug to Treat Transsphincteric Fistulas

Start date: November 2011
Phase:
Study type: Observational [Patient Registry]

This is a prospective clinical study on the efficacy of Gore-BioA fistula plug in high transsphincteric fistulas. Follow-up time is six months

NCT ID: NCT01478139 Recruiting - Clinical trials for Extracellular Matrix Alteration

Ligation of Intersphincteric Fistula Tract (LIFT) Versus LIFT-plug Procedure for Anal Fistula Repair

LIFT-plug
Start date: February 2011
Phase: Phase 3
Study type: Interventional

The purpose of this study is to validate the effect of Ligation of Intersphincteric Fistula Tract (LIFT) Versus LIFT-plug procedure for Anal Fistula Repair.

NCT ID: NCT01462747 Completed - Perianal Fistulas Clinical Trials

Efficacy and Safety Study of a Medical Device (KULIST)to Treat Perianal Fistulas

Start date: December 2011
Phase: Phase 2
Study type: Interventional

The aim of this study is to evaluate the effects of rectally administered activated carbon (medical device KULIST) in chronic, uncomplicated, perianal fistulas.