NCT Number: NCT02361450
Retrograde Colonic Irrigation to Manage Spina Bifida Functional Digestive Sequelae: a Multicenter, Prospective, Randomized Controlled Trial
Spina Bifida is a developmental congenital disorder caused by the incomplete closing of the embryonic neural tube, leading to serious malformations of the nervous system. Caudal neuropore malformations almost always lead to sensory-motor deficits (including complete paraplegia) with orthopedic deformations, pressure sores, and pelvic/perineal neurological dysfunctions (affecting the bladder-sphincter, anorectal, and genital sphere).
The purpose of the study is to assess the efficacy of retrograde colonic irrigation associated with usual care (medical treatments, patient education) on anorectal dysfunction (incontinence and/or constipation), compared to usual care only.
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Notify MeKey information
Conditions
Age range
15 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Not applicable
Primary location
CHRU de Lille, Lille, France
About this study
Sphincter dysfunctions impair the quality of life and patients' self-esteem. However, defecation disorders are important issues the Spina Bifida National Reference Center has to deal with. Indeed, more than half of patients are concerned. These disorders are mainly due to fecal stasis. Treatments include laxatives and hygiene recommendations. Colonic irrigation can also be useful, especially to achieve colonic vacuity and improve continence. The use of intra-rectal balloon inflation probes and the control of instillation flow improved retrograde colonic irrigation efficacy. Nevertheless, this technique is currently not evaluated in young adults suffering from Spina Bifida functional digestive sequelae, who are mainly concerned by Malone enema.
The purpose of the study is to assess the efficacy of retrograde colonic irrigation associated with usual care (medical treatments, patient education) on anorectal dysfunction (incontinence and/or constipation), compared to usual care only.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- Patients aging at least 15 years old with Spina Bifida neurological pelvi-perineal sequelae, objected by neurologic exam , functional urinary and/or anorectal and/or neurophysiological data,
- Patients with NBD score above 9,
- Written and informed consent (Minor children may be included with the consent of the two parents).
Exclusion criteria
- Patients with psychiatric disorders, cognitive or intellectual disabilities compromising the assessment of primary outcome measure,
- Patients using currently irrigation colonic technique,
- Patients with functional colostomy, known anal or colorectal stenosis, colorectal cancer, acute or chronic inflammatory disease, recent anal or colorectal surgery for less than 3 months, polyp removal for less than 4 weeks, ischemic colitis.
- Patients with urinary trophic or orthopedic disease with planned surgery during inclusion or follow-up periods,
- Patients with progressive anal disease (suppuration, hemorrhoid or rectal prolapse)
- Patient with a hard follow-up ( judged by the investigator)
- Person involved in another clinical trial
- Pregnant women
- Person with a measure of legal protection (guardianship)
Treatment and study plan
Usual Care
OtherPrimary outcomes
-
Neurogenic Bowel Dysfunction (NBD) score
Time frame: Ten weeks after inclusion
Secondary outcomes
-
Questionnaire data of incontinence and constipation (Cleveland scores)
Time frame: Ten weeks after inclusion
-
Questionnaire data of incontinence and constipation (Cleveland scores)
Time frame: Twenty-four weeks after inclusion
-
Quality of life
Time frame: Ten weeks after inclusion
Quality of life will be assess by semi-quantified scales
-
Quality of life
Time frame: Twenty-four weeks after inclusion
Quality of life will be assess by semi-quantified scales
-
Self esteem (Rosenberg scale)
Time frame: Ten weeks after inclusion
-
Functional digestive score (NBD)
Time frame: Twenty-four weeks after inclusion
-
Cumulative time spent using restrooms
Time frame: Ten weeks after inclusion
Cumulative time spent using restrooms will be collected with a patient reported outcome questionnaire
-
Cumulative time spent using restrooms
Time frame: Twenty-four weeks after inclusion
Cumulative time spent using restrooms will be collected with a patient reported outcome questionnaire
-
Number of accidents of incontinence
Time frame: Ten weeks after inclusion
Number of accidents of incontinence will be collected with a patient reported outcome questionnaire
-
Number of accidents of incontinence
Time frame: Twenty-four weeks after inclusion
Number of accidents of incontinence will be collected with a patient reported outcome questionnaire
-
Number of incontinence guards used
Time frame: Ten weeks after inclusion
Number of incontinence guards used will be collected with a patient reported outcome questionnaire
-
Number of incontinence guards used
Time frame: Twenty-four weeks after inclusion
Number of incontinence guards used will be collected with a patient reported outcome questionnaire
-
Type of incontinence guards used
Time frame: Ten weeks after inclusion
Type of incontinence guards (panty liner, pad, nappy) used will be collected with a patient reported outcome questionnaire
-
Type of incontinence guards used
Time frame: Twenty-four weeks after inclusion
Type of incontinence guards (panty liner, pad, nappy) used will be collected with a patient reported outcome questionnaire
-
Number of stools
Time frame: Ten weeks after inclusion
Number of stools will be collected with a patient reported outcome questionnaire
-
Number of stools
Time frame: Twenty-four weeks after inclusion
Number of stools will be collected with a patient reported outcome questionnaire
-
Stools consistency
Time frame: Ten weeks after inclusion
Stools consistency will be collected with a patient reported outcome questionnaire
-
Stools consistency
Time frame: Twenty-four weeks after inclusion
Stools consistency will be collected with a patient reported outcome questionnaire
-
Symptoms experienced during defecation
Time frame: Ten weeks after inclusion
Symptoms experienced during defecation will be collected with a patient reported outcome questionnaire
-
Symptoms experienced during defecation
Time frame: Twenty-four weeks after inclusion
Symptoms experienced during defecation will be collected with a patient reported outcome questionnaire
-
Frequency of digital help during defecation
Time frame: Ten weeks after inclusion
The frequency of digital stimulation will be collected with a patient reported outcome questionnaire
-
Frequency of digital help during defecation
Time frame: Twenty-four weeks after inclusion
The frequency of digital stimulation will be collected with a patient reported outcome questionnaire
Sponsors and collaborators
Lead sponsor
Rennes University Hospital
Other
Registry information
Acronym: IRRICO
Important dates
- Study start
- 2015
- Primary completion
- 2019
- Study completion
- 2019
- First posted
- Feb 11, 2015
- Registry last updated
- May 24, 2023
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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