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Treatment of Anal Fistula With Lasercoagulation

Treatment of Anal Fistula With Laser Mediated Heat Coagulation Using Fistula Laser Closure (FiLaC)

Status
Suspended
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03017898
Enrollment
52
Registered
2017-01-11
Start date
2017-03-03
Completion date
2025-12-31
Last updated
2024-03-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anal Fistula, Fistula-In-Ano

Keywords

FiLaC, Fistula Laser Closure, Laser Coagulation

Brief summary

The purpose of this study is to determine whether treatment with laser coagulation is an effective and safe treatment option for patients with anal fistula

Detailed description

Treatment of anal fistula remains a challenge - the only truly effective treatment available (fistulotomy) involves very high rates of anal incontinence if performed on the majority of patients, and a vast number of alternative, sphincter-preserving treatments have been developed and evaluated in the past decades. The treatment of anal fistula with laser coagulation causes the fistula to collapse and subsequently heal, without having to add any external materials. The available published studies show that the treatment is safe regarding infection and incontinence, and that a majority of the patients treated show complete healing. There is however a need for more prospective studies to ascertain these preliminary facts.

Interventions

Laser coagulation of anal fistula

Sponsors

Region Skane
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

1. Subject has been informed of the nature of the study, agrees to its provisions, and has provided written informed consent. 2. Subject must be at least 18 years of age 3. Subject must have a verified anal fistula (by transanal ultrasound performed by treating surgeon) 4. Subject must have a clean and infection-free fistula tract (no cavities seen on transanal ultrasound) 5. Subject must be able to comply with study and study follow-up requirements.

Exclusion criteria

1. Subject with anorectal fistula due to Crohn's disease 2. Subject has an undrained abscess in fistula tract (cavities as seen on transanal ultrasound) 3. Subject has fistula with side tracts (as seen on transanal ultrasound) 4. Subject is unable or unwilling to provide informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Healing12 monthsFistula closure success at 12 months is defined as complete healing of the fistula tract and external opening at clinical examination and on a transanal ultrasound performed by the examining surgeon (yes/no).

Secondary

MeasureTime frameDescription
Infection12 monthsRate of infection i.e. formation of abcess during the time of healing or thereafter within the first year of treatment.
Incontinence12 monthsPresence of fecal incontinence as described by the patient

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026