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

About this trial
This is an interventional treatment trial for Chronic Constipation Symptoms
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
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
NCT ID
NCT02381665
First Posted
February 13, 2015
Last Updated
March 2, 2015
Sponsor
Assistance Publique Hopitaux De Marseille
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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