Interferential therapy for chronic constipation in adults: The CON‐COUR randomizedcontrolled trial

Author:

Vitton Veronique1ORCID,Mion François2ORCID,Leroi Anne‐Marie345,Brochard Charlène6,Coffin Benoit78,Zerbib Frank9,Damon Henri2,Melchior Chloé3ORCID,Duboc Henri78,Queralto Michel10,Baumstarck Karine11

Affiliation:

1. Gastroenterology Unit Assistance Publique‐Hôpitaux de Marseille Aix‐Marseille Université Marseille France

2. Digestive Physiology Department Université de Lyon Hospices Civils de Lyon INSERM U1032 Lyon France

3. Digestive Physiology Department Rouen University Hospital Rouen France

4. Nutrition, Brain and Gut Laboratory UMR 1073 Rouen University Rouen France

5. Rouen University Hospital INSERM CIC‐CRB 1404 Rouen France

6. Digestive Physiology Unit University Hospital of Rennes University of Rennes 1 CIC 1414 Rennes France

7. Gastroenterology Department DMU ESPRIT, Hôpital Louis‐Mourier Colombes France

8. University of Paris Paris France

9. Gastroenterology Department Hôpital Haut‐Lévêque Bordeaux France

10. Service de Colo‐Proctologie Clinique des Cèdres Cornebarrieu France

11. Service d’Epidémiologie et Economie en Santé Direction de la Recherche en Santé AP‐HM Marseille France

Abstract

AbstractBackgroundChronic constipation (CC) is a frequent condition, and the first‐line treatment includes dietary rules, the use of laxatives, and biofeedback for evacuation disorders. However, almost half of the patients are dissatisfied with their current treatment. We report the first double‐blind randomized multicenter trial assessing the effectiveness of transabdominal electrical stimulation by interferential therapy (IFT) in the treatment of CC in adults.MethodsA prospective, multicenter, randomized, double‐blind, sham‐controlled, parallel‐group, phase 3 trial was conducted at 7 centers in France. The primary endpoint was 8‐week efficacy as defined by the number of complete spontaneous bowel movements during the last 4 weeks of the 8‐week stimulation period. Secondary endpoints included the evaluation of the effects of IFT on symptoms (Patient Assessment of Constipation Symptoms questionnair (PAC‐SYM)), quality of life (QOL) (Patient Assessment of Constipation Quality of Life), Colonic transit time (CTT), anorectal manometry, and patient satisfaction.ResultsThe proportion of 8‐week responders was not significantly different between the two groups (73.2% in the IFT group vs. 67.1% in the sham group). After 8 weeks of stimulation, the mean overall PAC‐SYM score and the mean reduction in the overall PAC‐SYM score were significantly greater in the IFT group than in the sham group. No differences were observed concerning CTT, anorectal manometry, or patient satisfaction.ConclusionsAlthough the primary endpoint was not reached, IFT can significantly alleviate the symptoms and improve the QOL of CC patients. It can be assumed that new treatments require different modes of evaluation and that the assessment of patient‐reported outcomes may become a priority among therapeutic targets of CC.Trial registration number NCT02381665.

Publisher

Wiley

Subject

Gastroenterology,Oncology

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