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Efficacy of Interferential Therapy in Chronic Constipation (CON-COUR) (CON-COUR)

Primary Purpose

Chronic Constipation Symptoms

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Flexstim IF
Flexstim IF faked
Sponsored by
Assistance Publique Hopitaux De Marseille
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Constipation Symptoms

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Subject with a history of chronic constipation defined as:

  • two or fewer spontaneous, complete bowel movements per week for a minimum of 6 months before the screening visit*
  • or as a sensation of incomplete evacuation or straining during defecation with at least 25% bowel movements*
  • Subject with chronic constipation lasting for more than 6 months
  • Subject with chronic constipation refractory to medical treatment for at least 3 months (failure or intolerance of medical treatment)
  • Subject have to interrupt any laxative treatment but during the study, patients are allowed, in case of absence of bowel movements for 3 or more consecutive days, to take up 15 mg of bisacodyl (Dulcolax, Boerhinger Ingelheim) as rescue medication
  • Subjects affiliated to or beneficiary of a social security system
  • Subjects who have signed written informed consent

Exclusion Criteria:

  • - Minors or pregnant or breast-feeding women
  • Subject with chronic constipation secondary to anorectal malformations, to colorectal or anal organic lesions or to a pelvic floor disorder considered by the investigator as necessitating a surgical treatment (rectal prolapse exteriorized, rectocele, enterocele)
  • Subjects with current implanted cardiac pacemakers, defibrillators, cardiac pumps, spinal stimulators or other implanted electronic devices
  • Subject with chronic constipation secondary to drug, to neurologic, endocrine or metabolic disorders
  • Subject with a history of partial colectomy
  • Subject with megacolon, megarectum, colonic inertia
  • Skin lesions preventing the installation of the electrodes
  • Women without effective contraception (hormonal or intra-uterine device)
  • Subject misunderstanding the written and spoken French
  • Subject participating in another biomedical research protocol

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Placebo Comparator

    Arm Label

    Group A

    Group B

    Arm Description

    Patient enrolled in this group will receive a device for effective interferential current stimulation.

    Patient enrolled in this group will receive a device that does not deliver current stimulation

    Outcomes

    Primary Outcome Measures

    Number of stool
    Assessing the short-term efficacy of interferential therapy in adult patients with severe chronic constipation.

    Secondary Outcome Measures

    Full Information

    First Posted
    February 13, 2015
    Last Updated
    March 2, 2015
    Sponsor
    Assistance Publique Hopitaux De Marseille
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02381665
    Brief Title
    Efficacy of Interferential Therapy in Chronic Constipation (CON-COUR)
    Acronym
    CON-COUR
    Official Title
    INTERFERENTIAL THERAPY IN THE TREATMENT OF CHRONIC CONSTIPATION IN ADULTS: A RANDOMIZED MULTI-CENTER TRIAL
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    March 2015
    Overall Recruitment Status
    Unknown status
    Study Start Date
    March 2015 (undefined)
    Primary Completion Date
    March 2018 (Anticipated)
    Study Completion Date
    March 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Assistance Publique Hopitaux De Marseille

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    Chronic constipation is a strong public health problem. Its prevalence is about 15% in Western countries with a significant impact on quality of life and health care costs . Two subtypes of constipation can be identified: slow transit constipation (STC), characterized by impaired propulsion of stool and due to dysfunction of colonic smooth muscle (myopathy) or its innervation (neuropathy), or both; and evacuation disorders, characterized by difficulty or inability with stool expulsion. They include disorders of the anorectal function such as dyssynergic defecation, as well as structural disorders such as rectocele, descending perineum syndrome and rectal prolapse . The first line therapy of chronic constipation is based on medical treatment combined with laxatives and dietary rules. However, these treatments are often disappointing. In case of failure, few treatment options are currently available. Surgery can sometimes be discussed for intractable chronic constipation. Sub-total colectomy can be proposed in case of STC but is associated with a significant morbidity. In case of pelvic floor disorders, a specific surgical treatment can be indicated. However, surgery is invasive, has a significant morbidity and the results are inconsistent. Recently, some studies have assessed the efficacy of sacral neuromodulation in the treatment of chronic constipation with some success, but this technique is expensive and requires the surgical implantation of a medical device . More recent works, including a randomized trial have showed, in children, the efficacy of interferential current stimulation in the treatment of chronic transit constipation . This treatment is used daily, at home, and uses four adhesive surface electrodes, two abdominal (placed below the costal margin) and two paraspinal (placed between T9 and L2) producing two sinusoidal currents crossing the body, 1 hour per day for 1-3 months. To date, only one open-label study has evaluated this technique in adults and has shown encouraging results in three months with an efficiency on 7/11 patients (63.6%) in the number of stools, severity score of constipation, quality of life's score associated with improved bowel transit time measured by radio-markers. Interferential therapy is a new treatment that has demonstrated its efficiency in the treatment of chronic constipation in children. Our team has published the first and only pilot study in adults that also demonstrated encouraging results. These data are of particular interest since laxative treatments are often disappointing, are expensive and may have adverse events. This study would be the first randomized study to evaluate a non-invasive and non-pharmacological treatment of chronic constipation in adults. If its effectiveness is demonstrated, it will provide, for the first time, a new non-invasive step for patients with laxative treatment failure before considering surgical treatment.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Chronic Constipation Symptoms

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    200 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Group A
    Arm Type
    Experimental
    Arm Description
    Patient enrolled in this group will receive a device for effective interferential current stimulation.
    Arm Title
    Group B
    Arm Type
    Placebo Comparator
    Arm Description
    Patient enrolled in this group will receive a device that does not deliver current stimulation
    Intervention Type
    Device
    Intervention Name(s)
    Flexstim IF
    Intervention Description
    Patient enrolled will receive a device for effective interferential current stimulation
    Intervention Type
    Device
    Intervention Name(s)
    Flexstim IF faked
    Intervention Description
    Patient enrolled will receive a sham device.
    Primary Outcome Measure Information:
    Title
    Number of stool
    Description
    Assessing the short-term efficacy of interferential therapy in adult patients with severe chronic constipation.
    Time Frame
    8 weeks

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Subject with a history of chronic constipation defined as: two or fewer spontaneous, complete bowel movements per week for a minimum of 6 months before the screening visit* or as a sensation of incomplete evacuation or straining during defecation with at least 25% bowel movements* Subject with chronic constipation lasting for more than 6 months Subject with chronic constipation refractory to medical treatment for at least 3 months (failure or intolerance of medical treatment) Subject have to interrupt any laxative treatment but during the study, patients are allowed, in case of absence of bowel movements for 3 or more consecutive days, to take up 15 mg of bisacodyl (Dulcolax, Boerhinger Ingelheim) as rescue medication Subjects affiliated to or beneficiary of a social security system Subjects who have signed written informed consent Exclusion Criteria: - Minors or pregnant or breast-feeding women Subject with chronic constipation secondary to anorectal malformations, to colorectal or anal organic lesions or to a pelvic floor disorder considered by the investigator as necessitating a surgical treatment (rectal prolapse exteriorized, rectocele, enterocele) Subjects with current implanted cardiac pacemakers, defibrillators, cardiac pumps, spinal stimulators or other implanted electronic devices Subject with chronic constipation secondary to drug, to neurologic, endocrine or metabolic disorders Subject with a history of partial colectomy Subject with megacolon, megarectum, colonic inertia Skin lesions preventing the installation of the electrodes Women without effective contraception (hormonal or intra-uterine device) Subject misunderstanding the written and spoken French Subject participating in another biomedical research protocol
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Véronique VITTON, MD PhD
    Phone
    +33431964349
    Email
    veronique.vitton@ap-hm.fr
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Urielle DESALBRES
    Organizational Affiliation
    Assistance Publique Hopitaux De Marseille
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    26012788
    Citation
    Vitton V, Benezech A, Honore S, Sudour P, Lesavre N, Auquier P, Baumstarck K. CON-COUR study: Interferential therapy in the treatment of chronic constipation in adults: study protocol for a randomized controlled trial. Trials. 2015 May 28;16:234. doi: 10.1186/s13063-015-0752-8.
    Results Reference
    derived

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    Efficacy of Interferential Therapy in Chronic Constipation (CON-COUR)

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