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Seated Evaluation of Anorectal funcTion by High Resolution Anorectal Manometry

Seated Evaluation of Anorectal funcTion by High Resolution Anorectal Manometry: a Randomized Comparison of Measurements in the Seated and Left Lateral Positions

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02633592
Acronym
SEAT
Enrollment
60
Registered
2015-12-17
Start date
2014-11-30
Completion date
2015-11-30
Last updated
2015-12-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Anismus, Incontinence

Keywords

High Resolution Anorectal Manometry, Magnetic Resonance Imaging, Balloon Expulsion, Position

Brief summary

To assess whether HR-ARM (High resolution Anorectal Manometry) performed in the more naturalistic / physiological upright, seated position on a commode provides a more valid assessment of anorectal function and simulated defecation than the same test performed in the standard, left lateral position

Detailed description

High Resolution Anorectal Manometry (HR-ARM) with data presented as pressure topography is a recent addition to the tests available for diagnosis of defecatory disorders including fecal incontinence and constipation.HR-ARM represents an advance on conventional manometry because closely spaced sensors across the anal sphincter remove the need for a pull-through procedure and facilitate data acquisition and interpretation. In particular measurements are not confounded by changes in position of the catheter relative to anal sphincter that occur during voluntary contraction and, especially, simulated defecation. Notwithstanding these technological improvements, important concerns remain about the validity of manometry measurements during simulated defecation. These concerns are based on the observation in both conventional and HR-ARM that a large proportion of healthy individuals appear to have abnormal anorectal function (dyssynergia) during simulated defecation.This limitation led to the recommendation that the finding of dyssynergia on manometry should be confirmed by defecography. This is unsatisfactory as diagnostic tests should not have a high rate of false positives and also because this increases the time and costs needed to complete diagnostic investigation in patients with defecatory disorders. The high rate of abnormal findings in healthy individuals may be because current manometry procedures and other anorectal tests (e.g. rectal balloon expulsion) are usually performed, not in the upright, seated position (USP) usually adopted for defecation, but in the un-physiological left lateral position (LLP). Several factors may contribute. First, defecation in the LLP is not aided by gravity as it is in the sitting position. Second, anorectal anatomy may be altered and less conducive to the passage of stool in the LLP. Third, simulating defecation in the LLP does not reflect normal behavior and, despite optimal interaction and explanation by the investigator, changes in patient behavior may result in apparent dyssynergia Finally, social stress, related to proximity of the investigator observing defecation, makes individuals feel unable to strain at stool or attempt defecation. A simple probe holder device that, by adhering to the skin is positioned at the natal cleft to support the ManoScan HR ARM catheter can be used to assess anorectal pressures in the sitting position (both produced by Given Imaging, Yoqeam, Israel). This simple device stabilizes the catheter position when the patient is in USP on a commode and allows the investigator to withdraw behind the curtains of the examination cubicle.

Interventions

OTHERHRARM

Patients and healthy volunteers are investigated in the seated and lying position during HRAM

OTHERMRI Defecography

Patients and healthy volunteers are investigated in the supine and left lateral position in the MRI

Sponsors

University of Zurich
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
Yes

Inclusion criteria

Inclusion criteria: All * Signed informed consent * Male or female, age 18 - 75 years * Females eligible to participate either if physiologically incapable of becoming pregnant or with a negative urine pregnancy test at screening * HS: Absence of symptoms of constipation or incontinence Patients with fecal incontinence * Passive or Urge Incontinence * Wexner Score of 5-20 (more than mild severity of incontinence) Patients with obstructive defecation • Cleveland Clinic Constipation Scoring System: 10-30 (more than mild severity of constipation)

Exclusion criteria

* • Participation in any other clinical trial with investigational or approved drugs within the last month before the study * Significant medical, surgical or psychiatric disease requiring on-going active management * Previous gastrointestinal or gynaecological disease (exception: non symptomatic ovarian cysts, occasional reflux, appendectomy, hysterectomy, cholecystectomy) * Regular use of opiates or other constipating agents * Presence of fecal impaction on clinical per rectal exam * Abnormal findings on proctoscopy / endoscopy (e.g. Inflammatory Bowel Disease, neoplasm, acute or chronic anal fissure, large haemorrhoids (grade 3-4) intussusception, prolapse or gross perineal descent (\>5cm) on straining * Insufficient understanding of German language to comply with instructions * Contraindication for MRI: Presence of non-MR-compatible metallic implants, devices or metallic foreign bodies

Design outcomes

Primary

MeasureTime frameDescription
Recto-anal pressure gradient (RAPG)1 hourRAPG change in the LLP and sitting position (mmHg)

Secondary

MeasureTime frameDescription
Presence of dyssynergia on HR-ARM1 hourRAPG of -40mmHg or lower
Presence of dyssynergic defecation on MRI in healthy controls1 hourparadox contraction or no opening of the anal canal
Agreement of MR findings in different body positions with HR-ARM findings1 hourdiagnostic concordance of the two investigations
Patient positional preference1 hourCategorical (forced choice) LLP vs. SEAT

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026