Treatment of Anal Fistula With Lasercoagulation

Sponsor
Region Skane (Other)
Overall Status
Suspended
CT.gov ID
NCT03017898
Collaborator
(none)
52
1
1
93
0.6

Study Details

Study Description

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

Condition or Disease Intervention/Treatment Phase
  • Procedure: Laser Coagulation
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
52 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Treatment of Anal Fistula With Laser Mediated Heat Coagulation Using Fistula Laser Closure (FiLaC)
Actual Study Start Date :
Mar 3, 2017
Anticipated Primary Completion Date :
Dec 1, 2023
Anticipated Study Completion Date :
Dec 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Laser coagulation

Treatment of anal fistulae meeting the inclusion criteria

Procedure: Laser Coagulation
Laser coagulation of anal fistula
Other Names:
  • Fistula Laser Closure (FiLaC)
  • Outcome Measures

    Primary Outcome Measures

    1. Healing [12 months]

      Fistula 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 Outcome Measures

    1. Infection [12 months]

      Rate of infection i.e. formation of abcess during the time of healing or thereafter within the first year of treatment.

    2. Incontinence [12 months]

      Presence of fecal incontinence as described by the patient

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts 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.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Skåne University Hospital Malmo Sweden

    Sponsors and Collaborators

    • Region Skane

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Region Skane
    ClinicalTrials.gov Identifier:
    NCT03017898
    Other Study ID Numbers:
    • FiLaC-2016
    First Posted:
    Jan 11, 2017
    Last Update Posted:
    Jan 31, 2022
    Last Verified:
    Jan 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Region Skane
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 31, 2022