Defecation Patterns in Constipated Patients
Constipation by Outlet Obstruction
About this trial
This is an interventional diagnostic trial for Constipation by Outlet Obstruction focused on measuring Obstructed defecation, Pelvic floor dysynergia, Paradoxical contraction of the anal sphincter, Anorectal motility, Impedance planimetry of anal sphincter
Eligibility Criteria
Inclusion Criteria: Two groups of subjects will be studied - normal healthy subjects and patients with chronic constipation.
Normal subjects:
Inclusion criteria *Normal defecation pattern, i.e., bowel movement once every day or other day without excessive straining and sense of complete evacuation.
Exclusion Criteria:
- Subjects not willing to consent and undergo the specified tests in this study
- Pregnant women
- Subjects with concurrent fecal incontinence and constipation symptoms
- Chronic diseases
- Taking medications that affect anorectal function
- History of anorectal surgery or bowel resection.
Constipation patients:
Inclusion Criteria:
Rome IV diagnostic criteria will be used to diagnose chronic constipation. Patients must have experienced at least two of the following symptoms over the preceding 3 months:
- Fewer than three spontaneous bowel movements per week,
- Straining for more than 25% of defecation attempts,
- Lumpy or hard stools for at least 25% of defecation attempts, and
sensation of anorectal obstruction or blockage.
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Exclusion Criteria:
- Patients not willing to consent and undergo the specified tests in this study
- pregnant women and patients with concurrent fecal incontinence
- History of anorectal surgery or bowel resection.
Sites / Locations
- University of California San DiegoRecruiting
Arms of the Study
Arm 1
Arm 2
Experimental
Experimental
Effect of atropine on the defecation
Effect of bisacodyl on the defecation
Atropine is an anticholinergic drug and expected to inhibit rectal contractions and inhibit evacuation of the rectal balloon. Each subject will be studied twice once with and once without atropine.
Bisacodyl is a stimulant of rectal contraction and expected to facilitate evacuation of rectal balloon (fecobionics device). Each subject will be studied twice, once with and once without bisacodyl.