search
Back to results

Anal Fistula Plug for High-type Anal Fistulae

Primary Purpose

High-type Anal Fistulae

Status
Terminated
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Anal fistula plug
Sponsored by
Chinese University of Hong Kong
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for High-type Anal Fistulae focused on measuring Anal fistula, High-type, Anal fistula plug, Efficacy, Recurrence

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with high-type anal fistulae confirmed by MRI
  • Informed consent available

Exclusion Criteria:

  • Patients with previous fistula surgery
  • Patients with Crohn's disease
  • Patients allergic to porcine material

Sites / Locations

  • Department of Surgery, Prince of Wales Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Anal fistula plug

Arm Description

Outcomes

Primary Outcome Measures

Fistula healing rate and time for fistula closure

Secondary Outcome Measures

Fistula recurrence rate
Morbidity

Full Information

First Posted
June 13, 2007
Last Updated
February 12, 2014
Sponsor
Chinese University of Hong Kong
search

1. Study Identification

Unique Protocol Identification Number
NCT00487071
Brief Title
Anal Fistula Plug for High-type Anal Fistulae
Official Title
Efficacy of Anal Fistula Plug in the Management of High-type Anal Fistulae: a Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
February 2014
Overall Recruitment Status
Terminated
Why Stopped
No financial support
Study Start Date
August 2006 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
February 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Chinese University of Hong Kong

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The aim of this pilot study is to evaluate the efficacy and safety of anal fistula plug in the management of high-type anal fistulae among Hong Kong Chinese patients.
Detailed Description
An anal fistula is an abnormal communication between the anal or rectal lumen and the perianal skin. Anal fistulae are described according to the level at which they transgress the anal sphincter. If the internal opening begins above the anal sphincter then the fistula is described as 'high'. Traditional surgery for high-type anal fistulae often requires staged operations with fistulotomy and seton insertion. The surgery usually results in large and deep wounds which can take months to heal. Moreover, risk of faecal incontinence is inevitable because part of the anal sphincter is divided during the surgery. The Surgisis® anal fistula plug is a minimally invasive and sphincter-preserving alternative to traditional fistula surgery. It is a newly developed biomaterial made from complex collagen obtained from pigs - animals that have a collagen structure almost identical to that of human tissue. During manufacturing of the plug, living cells are removed by special processes to help ensure that no transmittable diseases are present in the tissue. The plug is a conical device and is placed by drawing it through the fistula tract and suturing it in place. As pig collagen is so similar to human collagen, the plug, once implanted, incorporates naturally over time into the human tissue (human cells and tissues will 'grow' into the plug), thus facilitating the closure of the fistula. Preliminary clinical data from USA showed a high fistula closure rate of 87%. The anal fistula plug can also avoid protracted postoperative wound care and minimise the risk of faecal incontinence. We would like to carry out a pilot study, the aim of which is to evaluate the efficacy and safety of this new anal fistula plug in the management of high-type anal fistulae. This is believed to be the first study of its kind in Hong Kong. Patients with high-type anal fistulae confirmed by MRI will be recruited into this study. Patients with previous history of fistula surgery, patients with Crohn's disease, and patients with known allergy to porcine material will be excluded. EUA + anal fistula plug will be performed. Outcome measures include fistula healing rate, recurrence rate, and morbidity. Follow-up MRI will be arranged at 3 months and 6 months after the operation to objectively evaluate the healing of the fistulae.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
High-type Anal Fistulae
Keywords
Anal fistula, High-type, Anal fistula plug, Efficacy, Recurrence

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
10 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Anal fistula plug
Arm Type
Experimental
Intervention Type
Device
Intervention Name(s)
Anal fistula plug
Primary Outcome Measure Information:
Title
Fistula healing rate and time for fistula closure
Time Frame
Up to 1 year
Secondary Outcome Measure Information:
Title
Fistula recurrence rate
Time Frame
Up to 1 year
Title
Morbidity
Time Frame
Up to 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with high-type anal fistulae confirmed by MRI Informed consent available Exclusion Criteria: Patients with previous fistula surgery Patients with Crohn's disease Patients allergic to porcine material
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Simon SM Ng, FRCSEd (Gen)
Organizational Affiliation
Chinese University of Hong Kong
Official's Role
Principal Investigator
Facility Information:
Facility Name
Department of Surgery, Prince of Wales Hospital
City
Hong Kong SAR
Country
China

12. IPD Sharing Statement

Learn more about this trial

Anal Fistula Plug for High-type Anal Fistulae

We'll reach out to this number within 24 hrs