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Fistura® Procedure for the Treatment of Complex Anal Fistulas

D

Dr Benjamin NEBBOT

Status

Suspended

Conditions

Complex Anal Fistulas

Treatments

Device: Fistura® Procedure

Study type

Interventional

Funder types

Other

Identifiers

NCT05899569
Fistura

Details and patient eligibility

About

This study aims to evaluate the healing rate of complex fistulas using radiofrequency (Fistura® procedure), in a prospective, interventional, monocenter, single-arm design.

Full description

Perianal fistula is a rare disease characterized by a tract that connects the perineal skin to the anal canal. These fistulas usually lead to anal pain, intermittent anal purulent discharge and abscess recurrence. The choice of the treatment depends on the type of fistula, simple or complex fistulas. Simple fistulas are defined as inter-sphincteric and trans-sphincteric fistulas involving less than 30 % of the external sphincter. Complex anal fistulas include trans-sphincteric fistulas involving more than 30% of the external sphincter, supra-sphincteric fistulas, extra-sphincteric fistulas, horseshoe fistulas or fistulas involving multiple tracts, anal fistulas associated with inflammatory bowl disease, radiation, malignancy, preexisting fecal incontinence or chronic diarrhea. While treatments in one stage (including fistulotomy (laying open the fistula tract) and fistulectomy (excision of the fistula tract) have shown an acceptable benefit (healing) / risk (incontinence) balance for the treatment of simple fistulas and have become the treatment of choice, there is a risk of incontinence in up to 80 % of patients with a complex fistula after one stage treatment. Alternative "sphincter-saving techniques" have been developed. However, none have shown evidence of superiority in terms of healing rate or anal incontinence. It therefore seems appropriate to develop new treatment alternatives for patients with a complex anal fistula. The clinical investigation is designed to evaluate the global healing rate of complex anal fistulas after radiofrequency procedure using the Fistura® procedure. Healing rate will be evaluated clinically and by performing an MRI. Secondary outcomes include healing rate per type of fistulas, assessment of anal incontinence, energy used and duration of the procedure, return to daily activities and work, quality of life and postoperative complications.

Enrollment

50 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patients with complex fistulas.

Complex fistulas include trans-sphincteric fistulas involving more than 30 % of the external sphincter, supra-sphincteric fistulas, extra-sphincteric fistulas, horseshoe fistulas or fistulas involving multiple tracts (according to the ASCRS) for which:

Suppuration is described by the patient and/or visible by an opening in the anal margin or by anoscopy Clinical symptoms led to an MRI demonstrating the path

Fistula path demonstrated in the acute phase during drainage of an abscess

Patient ≥ 18 years at study entry Patients with a previously drained fistula, without diverticula > 10 mm, without T2 hyperintensity (assessed by MRI). Drainage is achieved by placing a seton from 10 weeks to 12 months prior to the procedure. Patient and investigator signed and dated the informed consent form prior to the procedure

Exclusion criteria

Patient < 18 years at study entry Patient has a known contraindication to treatment using radiofrequency (infectious anal pathologies, anal fissures, residual Longo anterior treatment staples) Patient has a known contraindication to MRI Simple fistulas defined as inter-sphincteric or trans-sphincteric, involving less than 30 % of the total height of the sphincter apparatus (attested by MRI, ASCRS classification) Patient has a fistula associated with radiation and inflammatory bowel disease Patient is unable/unwilling to provide informed consent Patient is unable to comply with the protocol or proposed follow-up visits and questionnaires Patient is currently participating in another clinical study

Trial design

50 participants in 1 patient group

Fistura procedure
Experimental group
Description:
Adults participants with complex anal fistulas.
Treatment:
Device: Fistura® Procedure

Trial contacts and locations

1

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Central trial contact

Clotilde Thumser-Henner, PhD

Data sourced from clinicaltrials.gov

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