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Completed

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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Key information

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

Retrograde Colonic Irrigation

Device

Usual Care

Other

Primary outcomes

  1. Neurogenic Bowel Dysfunction (NBD) score

    Time frame: Ten weeks after inclusion

Secondary outcomes

  1. Questionnaire data of incontinence and constipation (Cleveland scores)

    Time frame: Ten weeks after inclusion

  2. Questionnaire data of incontinence and constipation (Cleveland scores)

    Time frame: Twenty-four weeks after inclusion

  3. Quality of life

    Time frame: Ten weeks after inclusion

    Quality of life will be assess by semi-quantified scales

  4. Quality of life

    Time frame: Twenty-four weeks after inclusion

    Quality of life will be assess by semi-quantified scales

  5. Self esteem (Rosenberg scale)

    Time frame: Ten weeks after inclusion

  6. Functional digestive score (NBD)

    Time frame: Twenty-four weeks after inclusion

  7. 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

  8. 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

  9. 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

  10. 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

  11. 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

  12. 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

  13. 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

  14. 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

  15. Number of stools

    Time frame: Ten weeks after inclusion

    Number of stools will be collected with a patient reported outcome questionnaire

  16. Number of stools

    Time frame: Twenty-four weeks after inclusion

    Number of stools will be collected with a patient reported outcome questionnaire

  17. Stools consistency

    Time frame: Ten weeks after inclusion

    Stools consistency will be collected with a patient reported outcome questionnaire

  18. Stools consistency

    Time frame: Twenty-four weeks after inclusion

    Stools consistency will be collected with a patient reported outcome questionnaire

  19. Symptoms experienced during defecation

    Time frame: Ten weeks after inclusion

    Symptoms experienced during defecation will be collected with a patient reported outcome questionnaire

  20. Symptoms experienced during defecation

    Time frame: Twenty-four weeks after inclusion

    Symptoms experienced during defecation will be collected with a patient reported outcome questionnaire

  21. 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

  22. 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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