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Endoscopic Treatment of Complex Anal Fistulas (VAAFT)

Primary Purpose

Anal Fistula

Status
Terminated
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
operation
VAAFT
Sponsored by
University of Southern Denmark
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Anal Fistula focused on measuring VAAFT, anal fistula, sphincter reconstruction

Eligibility Criteria

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

Inclusion Criteria:

  • Patients with complex transsphincteric anal fistulas >18 yrs old.

Exclusion Criteria:

  • Crohns fistulas
  • Signs of suppuration or/and branching.
  • Malignancy within 5 yrs.
  • Previous radiotherapy of the abdomen and pelvis.
  • Current Immune- suppressive treatment.

Sites / Locations

  • Odense University Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Operation

VAAFT

Arm Description

the fistula will be excised after dividing the sphincter and primary reconstruction .

the fistula tract will be visualized by scope, closing the internal opening with absorbable sutures.

Outcomes

Primary Outcome Measures

The recurrence rate of perianal fistula
A comparison on the rate of recurrence of anal fistula in each group will be performed by t-test. A p-value of less than 0.05 will be considered as statistical significant.

Secondary Outcome Measures

changes in quality of life score
A comparison on changes in quality of life, using The Short Form (36) Health Survey in each group will be performed by t-test. A p-value of less than 0.05 will be considered as statistical significant.
changes in fecal incontinence score
A comparison on changes in Wexner score in each group will be performed by t-test. A p-value of less than 0.05 will be considered as statistical significant.
changes in manometric study
A comparison on changes in manometric study(including maximum resting pressure, maximum squeeze pressure) in each group will be performed by t-test. A p-value of less than 0.05 will be considered as statistical significant.

Full Information

First Posted
October 20, 2015
Last Updated
May 11, 2021
Sponsor
University of Southern Denmark
Collaborators
Odense University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT02585167
Brief Title
Endoscopic Treatment of Complex Anal Fistulas
Acronym
VAAFT
Official Title
Endoscopic or Surgical Treatment of Complex Perianal Fistula. A Randomized Controlled Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2021
Overall Recruitment Status
Terminated
Why Stopped
The significantly higher recurrence rate in the intervention group led to a serious ethical consideration of a premature closing of the study which was decided due to safety and benefit concerns
Study Start Date
February 2016 (Actual)
Primary Completion Date
May 2021 (Actual)
Study Completion Date
May 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Southern Denmark
Collaborators
Odense University Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This is a randomised controlled trial to evaluate the outcome of treatment of complex perianal fistula by Video-assisted anal fistula treatment (VAAFT) compared to fistulectomy and sphincter reconstruction as standard surgical procedure.
Detailed Description
The surgical treatment of complex fistulas is difficult and ideally aims to completely heal the fistula and prevent recurrence without affecting the anal sphincter function. The definitive surgical treatment options include transsphincteric fistulectomy and sphincter repair, intersphincteric ligation of the fistula tract (LIFT), transanal advancement flap and cutting Seton suture. All the methods caries a relative high recurrence and complication rate including the risk of anal incontinence .Transsphincteric fistulectomy and primary reconstruction of the anal sphincter has been reported to have a healing rate between 90 - 95,8 %, recurrence rate of 7,1-9,7 % and 5-30 % experience incontinence in varying degree. Video-assisted anal fistula treatment (VAAFT) is a novel sphincter saving procedure for treating complex anal fistulas and recently introduced with promising early results with a healing rate of 74-87.1 % after 1 year. The procedure can be done as a day-case surgery with the ability of precise identification of the fistula tract, including the presence of secondary branches. The method includes an endoscopic debridement and closure of the internal opening. Only few scientific reports of the method has been published and only with short term results, and there is a need of validating the efficacy of this procedure in a prospective randomized trial. There are few randomised controlled trials in the literature on the treatment of complex anal fistulas treatment and there is no conclusive evidence of which method is the best. Furthermore the knowledge of changes in quality of life and functional results in terms of standardized continence evaluation and manometric studies are either contradictive or simply lacking after the surgery for anal fistulas. The aim of this study is to conduct a randomized clinical trial to compare VAAFT (mini invasive and sphincter-saving) with the traditional transsphincteric fistulectomy and primary reconstruction in terms of recurrence rate, manometric and functional changes as well as changes in quality of life.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anal Fistula
Keywords
VAAFT, anal fistula, sphincter reconstruction

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
47 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Operation
Arm Type
Active Comparator
Arm Description
the fistula will be excised after dividing the sphincter and primary reconstruction .
Arm Title
VAAFT
Arm Type
Experimental
Arm Description
the fistula tract will be visualized by scope, closing the internal opening with absorbable sutures.
Intervention Type
Procedure
Intervention Name(s)
operation
Other Intervention Name(s)
Fistulectomy and primary sphincter reconstruction
Intervention Description
the fistula will be excised after dividing the sphincter and primary reconstruction will be performed with absorbable sutures, closing the internal opening and leaving the external opening unclosed for drainage.
Intervention Type
Device
Intervention Name(s)
VAAFT
Intervention Description
Karl Storz Video Equipment is used. The fistula tract will be visualized from the external to the internal opening, closing the internal opening with absorbable sutures, then brushing and cauterization of the tract(s) leaving the external opening unclosed for drainage.
Primary Outcome Measure Information:
Title
The recurrence rate of perianal fistula
Description
A comparison on the rate of recurrence of anal fistula in each group will be performed by t-test. A p-value of less than 0.05 will be considered as statistical significant.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
changes in quality of life score
Description
A comparison on changes in quality of life, using The Short Form (36) Health Survey in each group will be performed by t-test. A p-value of less than 0.05 will be considered as statistical significant.
Time Frame
baseline and 6 months
Title
changes in fecal incontinence score
Description
A comparison on changes in Wexner score in each group will be performed by t-test. A p-value of less than 0.05 will be considered as statistical significant.
Time Frame
baseline and 6 months
Title
changes in manometric study
Description
A comparison on changes in manometric study(including maximum resting pressure, maximum squeeze pressure) in each group will be performed by t-test. A p-value of less than 0.05 will be considered as statistical significant.
Time Frame
baseline and 6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with complex transsphincteric anal fistulas >18 yrs old. Exclusion Criteria: Crohns fistulas Signs of suppuration or/and branching. Malignancy within 5 yrs. Previous radiotherapy of the abdomen and pelvis. Current Immune- suppressive treatment.
Facility Information:
Facility Name
Odense University Hospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark

12. IPD Sharing Statement

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Links:
URL
http://open.rsyd.dk/OpenProjects/da/openProject.jsp?openNo=145
Description
OPEN homepage

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Endoscopic Treatment of Complex Anal Fistulas

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