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Sacral Neuromodulation and Faecal Incontinence and Its Unknown Effect on the External Anal Sphincter

SFINX - Sacral Neuromodulation and Faecal Incontinence and Its Unknown Effect on the External Anal Sphincter

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06763861
Acronym
SFINX
Enrollment
15
Registered
2025-01-08
Start date
2024-12-09
Completion date
2028-12-31
Last updated
2025-01-08

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

Conditions

Fecal Incontinence

Keywords

Fecal Incontinence, Sacral neuromodulation, Surgery, Pathology, Proctology, Quality of Life, Health status

Brief summary

This innovative project aims to investigate structures and morphology of the external anal sphincter (EAS) as well as the impact of sacral neuromodulation (SNM) on the EAS morphology and biochemistry among patients with faecal incontinence (FI). SNM is a well implemented treatment for FI and consist of electrical stimulation of sacral nerve roots to promote continence and may even contribute to total continence. It has shown a positive effects on both short- and long-term. The biologic effect of SNM on EAS is unknown. The aim is to investigate the effect of SNM on EAS morphology, function, and biochemistry to help physicians and researchers to understand the underlying mechanisms of SNM and the anal sphincter complex to further improve and optimize treatment methods for patients with FI. The research project consists of three phases. The first phase includes biopsies from the EAS among patients with no previous history of FI. These patients have been diagnosed with rectal cancer and will undergo surgery with abdominoperineal excision. The second phase includes patients diagnosed with FI and subject for implantation of SNM for treatment of FI. Prior to implantation of SNM all patients will have been examined with 3D endo-anal ultrasound and anorectal manometry as well as answered questionnaires targeting general health, bowel dysfunction and FI. A biopsy of the superficial portion of the EAS is retrieved under local anaesthesia in connection to the test period for implantation of the SNM device. The last phase, phase three, includes 3D endo-anal ultrasound, anorectal manometry, and a second biopsy of the EAS twelve months after implantation with SNM. The histopathological analysis in all the three phases will include general morphology, distribution of cell nuclei, satellite cells, muscle fiber type, neural structures and connective tissue.

Interventions

OTHERBiopsy

Biopsies from EAS

Sponsors

Umeå University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

Phase 1 Inclusion Criteria: * ≥ 18 years of age * Male or female * Diagnosed with rectal cancer and receive treatment with abdominoperineal resection * Signed an informed consent

Exclusion criteria

* Previous diagnosis of FI * Unable to speak and/or read Swedish to ensure informed consent * Tumour involving the sphincter complex or is in close connection Phase 2 and 3 Inclusion Criteria: * Diagnosed with FI and will receive treatment with sacral neuromodulation * Male or female * Signed an informed consent

Design outcomes

Primary

MeasureTime frame
The effect of sacral neuromodulation on the external anal sphincter muscle among patients with faecal incontinence2 years - The biopsies will be analysed and assessed continuously.

Countries

Sweden

Contacts

Primary ContactStrigård, Prof., Senior consultant
karin.strigard@umu.se+46(0)90 785 00 00
Backup ContactLouise Almkvist, MD
louise.almkvist@umu.se+46(0)90 785 00 00

Outcome results

None listed

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