Laser Assisted Treatment of Fistula In Ano (LATFIA)
Primary Purpose
Fistula in Ano, Rectal Fistula
Status
Recruiting
Phase
Not Applicable
Locations
Belgium
Study Type
Interventional
Intervention
Laser treatment of anal fistula
RAF
Sponsored by
About this trial
This is an interventional treatment trial for Fistula in Ano focused on measuring Rectal, Advancement Flap, Laser assisted Fistula Closure, Randomised Control Trial
Eligibility Criteria
Inclusion Criteria:
- Patients with fistula involving more than one-third of the external anal sphincter
- Single, continuous fistula tract at time of inclusion
- Loose seton present in fistula tract for 2 months or more at time of inclusion
- Age ≥ 18
- Able to complete an informed written consent, understand its implications and contents, and participate in follow-up
Exclusion Criteria:
- Fistula tract < 1 cm
- Complex fistula tract system (branching of fistula tract inside the sphincter complex)
- Pregnancy
- HIV-positive
- Crohn´s disease, Ulcerative colitis
- Fistula due to malignancy
- Tuberculosis
- Hidradenitis Suppurativa
- No internal opening
- Unable to undergo or contraindications to MRI
Sites / Locations
- Antwerp University HospitalRecruiting
- Az St Dimpna GeelRecruiting
- Jessa Ziekenhuis HasseltRecruiting
- Gent University Hospital
- Brussels University Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
Laser assisted fistula closure
Rectal advancement flap
Arm Description
Group to be actively treated with laser assisted fistula surgery
Group to be actively treated with a rectal advancement flap.
Outcomes
Primary Outcome Measures
Primary fistula closure after index laser or flap treatment
Success rate (number of patients) of laser/flap treatment defined as full healing (fistula closure) after the index procedure
Secondary Outcome Measures
Secondary Fistula closure
Secondary success rate (number of patients) defined as full healing (fistula closure) after a second procedure (either rectal advancement flap, laser treatment, fistulotomy)
Postoperative Pain
Reported pain after laser or flap treatment: measured using the visual analog scale - VAS where 0 = no pain; 10 = worst pain imaginable,
Postoperative fecal incontinence
Reported fecal incontinence after laser or flap treatment:
measured using the Vaizey score where minimum score 0 = perfect continence; maximum score 24 = totally incontinent)
Postoperative wound complications
Reported wound complications after laser or flap treatment defined as wound dehiscence or bleeding as reported on the adverse event forms
Postoperative Quality of Life
General postoperative well being and ability to partake in daily life and daily tasks (specific role functioning) measured and scored using the SF 36 questionnaire (consisting of 8 weighted scales:
vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role, functioning, and mental health. The lower the score the more disability. The higher the score the less disability)
This outcome is measured in all participants after the initial procedure (index flap or laser treatment) as well as after a second procedure (in case of recurrence)
Primary Recurrence
Number of participants presenting with a clinical recurrence or residual fistula after initial and laser/flap treatment (index procedure)
Secondary Recurrence
Number of participants presenting with a clinical recurrence or residual fistula after the second procedure (Laser - Flap - Fistulotomy - Ligation of the fistula tract, video-assisted fistula treatment)
Identify predictive factors for clinical fistula healing to determine the treatment indications.
This outcome evaluates the correlations between patients'/ fistula's clinical characteristics and primary healing rates
Full Information
NCT ID
NCT05390151
First Posted
April 21, 2022
Last Updated
June 14, 2022
Sponsor
University Hospital, Antwerp
Collaborators
Universitair Ziekenhuis Brussel, University Hospital, Ghent, AZ St.-Dimpna Geel, Jessa Hospital
1. Study Identification
Unique Protocol Identification Number
NCT05390151
Brief Title
Laser Assisted Treatment of Fistula In Ano
Acronym
LATFIA
Official Title
LATFIA-trial: Laser Assisted Treatment of Fistula In Ano Randomized Controlled Trial Comparing FiLaCTM to Rectal Advancement Flap
Study Type
Interventional
2. Study Status
Record Verification Date
March 2022
Overall Recruitment Status
Recruiting
Study Start Date
March 1, 2022 (Actual)
Primary Completion Date
September 1, 2025 (Anticipated)
Study Completion Date
March 1, 2026 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Hospital, Antwerp
Collaborators
Universitair Ziekenhuis Brussel, University Hospital, Ghent, AZ St.-Dimpna Geel, Jessa Hospital
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Randomised Controlled Trial comparing Laser assisted closure of transsphincteric fistula to the rectal advancement flap.
Detailed Description
A prevalent and complex fistula type is the high transsphincteric (TS) fistula. It typically runs through the upper two-thirds of the external anal sphincter (EAS) and is, due to the high risk of fecal incontinence, not suitable for fistulotomy and sphincter sparing treatment is required. To be included in this trial the participants should have a single, continuous TS fistula of cryptoglandular origin, that is treated by loose seton drainage for at least 2 months and is mapped by MRI. Participants with IBD, hidradenitis suppurativa or a malignant fistula will be excluded. Intervention Fistula Laser Closing (FiLaCTM) (Biolitec, Germany) is an endofistular technique, using a radial-emitting laser fiber that emits laser light with a maximum penetration depth of 2 - 3 mm. It destroys both the crypt gland and the additional epithelial layer of the fistula without damaging the sphincter. The fiber is inserted until the internal opening, activated and pulled backwards slowly, allowing the laser to have its effect. The external opening is excised and the internal opening is closed with a single absorbable suture. Rectal advancement flap is currently the gold standard for sphincter sparing treatment of high transsphincteric fistulae. The fistula is cored out and an advancement flap is made of mucosa and submucosa. The opening of the fistula in the flap is excised, the residual internal opening is closed with absorbable suture and the flap is sutured below the fistula to the anoderm. The advancement flap is a difficult technique that requires a relatively large transanal dissection that results in postoperative pain and may lead to disturbances in continence. Preliminary results with the Filac technique show fistula healing rates comparable to the advancement flap. Due to its simplicity, speed and minimal invasiveness the investigators expect a benefit for the participants in terms of postoperative pain, operating time and quality of life.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Fistula in Ano, Rectal Fistula
Keywords
Rectal, Advancement Flap, Laser assisted Fistula Closure, Randomised Control Trial
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
176 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Laser assisted fistula closure
Arm Type
Active Comparator
Arm Description
Group to be actively treated with laser assisted fistula surgery
Arm Title
Rectal advancement flap
Arm Type
Active Comparator
Arm Description
Group to be actively treated with a rectal advancement flap.
Intervention Type
Procedure
Intervention Name(s)
Laser treatment of anal fistula
Other Intervention Name(s)
FiLAC - LAFT
Intervention Description
using a radial laserprobe to treat transsphincteric fistula
Intervention Type
Procedure
Intervention Name(s)
RAF
Other Intervention Name(s)
rectal advancement flap
Intervention Description
current golden standard in transsphincteric fistula surgery
Primary Outcome Measure Information:
Title
Primary fistula closure after index laser or flap treatment
Description
Success rate (number of patients) of laser/flap treatment defined as full healing (fistula closure) after the index procedure
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Secondary Fistula closure
Description
Secondary success rate (number of patients) defined as full healing (fistula closure) after a second procedure (either rectal advancement flap, laser treatment, fistulotomy)
Time Frame
6 months
Title
Postoperative Pain
Description
Reported pain after laser or flap treatment: measured using the visual analog scale - VAS where 0 = no pain; 10 = worst pain imaginable,
Time Frame
6 months
Title
Postoperative fecal incontinence
Description
Reported fecal incontinence after laser or flap treatment:
measured using the Vaizey score where minimum score 0 = perfect continence; maximum score 24 = totally incontinent)
Time Frame
6 months
Title
Postoperative wound complications
Description
Reported wound complications after laser or flap treatment defined as wound dehiscence or bleeding as reported on the adverse event forms
Time Frame
6 months
Title
Postoperative Quality of Life
Description
General postoperative well being and ability to partake in daily life and daily tasks (specific role functioning) measured and scored using the SF 36 questionnaire (consisting of 8 weighted scales:
vitality, physical functioning, bodily pain, general health perceptions, physical role functioning, emotional role functioning, social role, functioning, and mental health. The lower the score the more disability. The higher the score the less disability)
This outcome is measured in all participants after the initial procedure (index flap or laser treatment) as well as after a second procedure (in case of recurrence)
Time Frame
6 months
Title
Primary Recurrence
Description
Number of participants presenting with a clinical recurrence or residual fistula after initial and laser/flap treatment (index procedure)
Time Frame
6 months
Title
Secondary Recurrence
Description
Number of participants presenting with a clinical recurrence or residual fistula after the second procedure (Laser - Flap - Fistulotomy - Ligation of the fistula tract, video-assisted fistula treatment)
Time Frame
12 months
Title
Identify predictive factors for clinical fistula healing to determine the treatment indications.
Description
This outcome evaluates the correlations between patients'/ fistula's clinical characteristics and primary healing rates
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Patients with fistula involving more than one-third of the external anal sphincter
Single, continuous fistula tract at time of inclusion
Loose seton present in fistula tract for 2 months or more at time of inclusion
Age ≥ 18
Able to complete an informed written consent, understand its implications and contents, and participate in follow-up
Exclusion Criteria:
Fistula tract < 1 cm
Complex fistula tract system (branching of fistula tract inside the sphincter complex)
Pregnancy
HIV-positive
Crohn´s disease, Ulcerative colitis
Fistula due to malignancy
Tuberculosis
Hidradenitis Suppurativa
No internal opening
Unable to undergo or contraindications to MRI
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Sander Van Hoof, M.D.
Phone
+3238212434
Email
sander.vanhoof@uza.be
First Name & Middle Initial & Last Name or Official Title & Degree
Niels Komen, M.D. Phd
Phone
+3238215007
Email
niels.komen@uza.be
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Niels Komen, M.D. Phd
Organizational Affiliation
University Hospital, Antwerp
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Sander Van Hoof, M.D.
Organizational Affiliation
University Hospital, Antwerp
Official's Role
Principal Investigator
Facility Information:
Facility Name
Antwerp University Hospital
City
Edegem
State/Province
Antwerpen
ZIP/Postal Code
2610
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Niels Komen, MD PhD
Phone
+3238215007
Email
niels.komen@uza.be
Facility Name
Az St Dimpna Geel
City
Geel
State/Province
Antwerpen
ZIP/Postal Code
2440
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ben Gys, MD PhD
Facility Name
Jessa Ziekenhuis Hasselt
City
Hasselt
State/Province
Limburg
ZIP/Postal Code
3500
Country
Belgium
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bert Houben, MD
Facility Name
Gent University Hospital
City
Gent
State/Province
Oost- Vlaanderen
ZIP/Postal Code
9000
Country
Belgium
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Dirk Van De Putte, MD
Facility Name
Brussels University Hospital
City
Brussels
ZIP/Postal Code
1090
Country
Belgium
Individual Site Status
Not yet recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jasper Stijns, MD
12. IPD Sharing Statement
Plan to Share IPD
No
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Laser Assisted Treatment of Fistula In Ano
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