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.
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Notify MeKey information
Conditions
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
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
Seton Placement
ProcedurePrimary outcomes
-
Fistula healing
-
Treatment failure
Secondary outcomes
-
Time to fistula healing
-
Time to treatment failure
-
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.
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