About this trial
Constipation is a frequent symptom that is reported by more than 10% of the general population. In a few case, constipation is resistant to medical standard care, including osmotic and stimulant laxatives. The diagnosis of colonic inertia may be suspected in these patients although diagnostic criteria for colonic inertia may vary from one country to another. In France, the diagnosis of colonic inertia is based on manometric study of the colorectal contractile activity using manometric probe. Using conventional manometric catheters, severe alteration of the colorectal motility is found in a very small subset of patients, who may later benefit from surgery. The recent use of high resolution manometric probe allowed to map more precisely colorectal motility, but whether these new parameters are relevant remains to be assessed. The aim of this study is to assess the diagnostic performance of a new high resolution manometric probe by comparing healthy volunteers to patients suspected of colonic inertia.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Age between 18 and 65 years
chronic Constipation (> 6 months)
delayed colonic transit time > 100 h
normal colonoscopy
Disqualifiers
With colonic transit time <100h
Distal (with radio-opaque markers stasis in the rectum)
From organic origin
Recent (<6 mois)
Trial design
Parallel
Treatments tested in this trial
High resolution manometry
DeviceHigh resolution manometry
Treatment groups
Trial outcomes
Primary outcomes
Frequency of isolated propagated colonic contractions
Number of colonic contractions during 24 hours
Secondary outcomes
Speed of isolated propagated colonic contractions
Average speed of colonic contractions during 24 hours
Colonic transit time
Transit time will be measured during during the first 24 hours
Sponsors and contacts
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