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Treatment of Fecal Incontinence and Chronic Constipation With Low-volume Irrigation

A

Aarhus University Hospital

Status

Not yet enrolling

Conditions

Fecal Incontinence
Constipation

Treatments

Device: Low-volume irrigation

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The aim of this study is to investigate the efficacy of low-volume irrigation on bowel function among patients with fecal incontinence and/or chronic constipation (of heterogenous origin).

Full description

The aim of this study is to investigate the efficacy of low-volume irrigation on bowel function among patients with FI and/or CC (of heterogenous origin). Further, the aim is to investigate if low volume irrigation can change the negative impact that symptoms of FI and/or CC (of heterogenous origin) have on the patients' daily activities and QoL. Additionally, the aim is to investigate the short-term and long-term discontinuation rates in relation to treatment with low-volume irrigation. Finally, the aim is to investigate the daily time-consumption, the practical challenges and the side effects related to low-volume irrigation. The study period is six weeks and the participants will be instructed to irrigate once daily with Qufora IrriSedo MiniGo.

This study is an interventional study. Patients with FI and/or CC of heterogenous origin, seen in the Nurse-led Clinic for Bowel Dysfunction at the Pelvic Floor Unit, Aarhus University hospital, will be included. Patients will be offered transanal irrigation as a treatment option. Patients presenting with Bristol stool type 6-7 should be offered conservative treatment to optimize the stool consistency. If patients can be regulated to a Bristol stool type 1-5, they can be invited to participate in the study. If necessary, regulation of the stool consistency in patients presenting with Bristol stool type 1-2 is an option, before introducing transanal irrigation.

Enrollment

92 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Patients with FI, CC or co-existing FI and CC of heterogenous origin.
  • Positive Rome IV criteria for constipation and/or positive Rome IV criteria for fecal incontinence.
  • Patients with Bristol stool type 1-5 as their primary stool consistency.
  • 18 years.
  • Ability to understand written and spoken Danish (due to questionnaire validity).

Exclusion criteria

  • Prior use of transanal irrigation or mini enema.
  • Patients with chronic diarrhea (Bristol stool type 6-7).
  • Patients with neurogenic bowel dysfunction.
  • Participation in research conflicting with the current study.
  • Diseases treated with rectal or anal surgery (except minor rectal or anal surgery).
  • Physical disability that affects the ability to use QuforaÒ IrriSedo MiniGo.
  • Major psychiatric diagnoses.
  • Patients with constipation with a chronic opioid use or other medications inducing constipation.
  • Pregnancy or plans to become pregnant.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

92 participants in 1 patient group

Low-volume irrigation
Experimental group
Description:
The patients will be instructed to irrigate once daily at a fixed time for 6 weeks. The patients will be instructed to use the irrigation 30 min after breakfast, capitalizing on the gastrocolic response; however, should this not fit in with the individual's lifestyle, then an alternative time of the day may be used. Preferably shortly after a large meal. The patients should fill the pump with 180 milliliters (a full pump) and irrigate with a volume of 160 milliliters of water.
Treatment:
Device: Low-volume irrigation

Trial contacts and locations

0

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Central trial contact

Peter Christensen

Data sourced from clinicaltrials.gov

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