Skip to main content
OpenTrials
Completed

NCT Number: NCT00450671

Treatment of Perirectal Fistula With Cutting Seton vs. Collagen Plug

The purpose of this study is to determine if the collagen plug method heals perirectal fistulae as well as the conventional seton method.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

H.Claude Hudson Comprehensive Health Center, Los Angeles, California, United States

Loading trial locations.

About this study

Traditional treatments for transsphincteric perirectal fistulae rely upon an immediate (fistulotomy) or delayed (seton) transsection of the sphincter muscle possibly resulting in fecal incontinence, take a long time to heal, and/or are associated with significant failure rates (ex. fibrin glue).

Newer treatment concepts such as the collagen plug do not physically interrupt the sphincter muscle, avoid and minimize the risk of fecal incontinence, and decrease the time to fistula healing. Exciting initial reports have confirmed the collagen plug's utility in treating perirectal fistulae, but a systematic scientific comparison is needed to validate the new, less invasive plug method.

The primary goal of this study is to show that the collagen plug heals transsphincteric perirectal fistulae as well as the conventional seton method.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients that are undergoing surgery for perirectal fistulae by the USC Colorectal Group
  • Patients that are older than 18 years of age and are able to understand and sign consent
  • Patients that are suitable candidates for either seton or collagen plug placement

Exclusion criteria

  • Preoperative patient exclusion factors:
  • Pregnant patients
  • Patients with a tumor-related fistula
  • Patients with known allergies to porcine products
  • Patients with known Crohn's disease
  • Intraoperative patient exclusion factors:
  • Patients with an active purulent infection (pus draining from the fistula tract or abscess associated with the fistula tract) at the time of surgery
  • Patients with a large diameter fistula (>3mm)
  • Patients with a superficial fistula
  • Patients with a short fistula (<1 cm in length)

Treatment and study plan

Collagen Plug Placement

Procedure

Seton Placement

Procedure

Primary outcomes

  1. Fistula healing

  2. Treatment failure

Secondary outcomes

  1. Time to fistula healing

  2. Time to treatment failure

  3. Rates of postoperative fecal continence

Sponsors and collaborators

Lead sponsor

University of Southern California

Other

Registry information

Official study title

Seton Placement vs. Surgisis Anal Fistula Plug Insertion for Perirectal Fistula: A Prospective Randomized Study

Important dates

Study start
2007
Study completion
2013
First posted
Mar 22, 2007
Registry last updated
Mar 17, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.