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Non-invasive Assessment of Colonic Motility

Electro-Entero-Graphy (EEnG) for Non-invasive Diagnosis of Motility Disorders of the Bowel

Status
Terminated
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04624334
Acronym
non-CoMoti
Enrollment
34
Registered
2020-11-10
Start date
2021-02-25
Completion date
2022-05-12
Last updated
2022-05-19

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

Conditions

Colon Disease, Electroenterography, Functional Constipation, Hirschsprung Disease, Slow Transit

Brief summary

The current diagnostic process of colonic motility disorders often takes a long time and involves multiple invasive, painful and/or unnecessary diagnostic procedures. To improve this diagnostic process, the potential of Electro-Entero-Graphy (EEnG) is investigated. During the EEnG procedure, several surface electrodes are positioned (under ultrasound guidance) on the abdomen so that electrical activity originating in the colon can be measured. Measurements will be performed after a period of fasting (when the colon is 'silent') and just after a meal (when the colon is moving) in both participants suffering from colonic motility disorders and healthy controls. It is hypothesized that these measurements are an indication of colonic motility and can be used as a diagnostic tool for colonic motility disorders. It is also hypothesized that this EEnG procedure is not more burdensome than the Gold Standard procedures for diagnosing colonic motility disorders. This will be assessed using questionnaires.

Interventions

OTHERElektro-Entero-Graphy procedure

Fasting, after which pre- and postprandial EEnG measurements are performed.

OTHEREEnG Questionnaire

Filling out questionnaire about EEnG procedure.

OTHERGold Standard Questionnaire

Filling out questionnaire about Gold Standard diagnostic used to diagnose colonic motility disorder.

Sponsors

Radboud University Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

* All participants: * Age ≤ 11 years for babies and children * Age ≥ 18 years for adults. Patients * For babies/children: * suffering from surgically untreated HSCR as determined by a rectal biopsy, or * suspected of HSCR, for which a rectal biopsy is planned * For adults: Suffering from a (suspected,) surgically untreated functional colonic motility disorder (such as slow-transit constipation, idiopathic/therapy resistant constipation of the colon), as diagnosed previously or will be diagnosed in the near future using the gold standard method.

Exclusion criteria

* All participants: * For adults: BMI \> 27 kg/m2 * For babies/children: weight for length \> 2.5 standard deviations of WHO Child Growth Standard * Pregnancy * Diabetes * Any food intolerance * Presence of an intestinal stoma * Use of continuous tube feeding * Healthy controls: * The presence of any known gastro-intestinal conditions * Use of laxatives in the past two years * Participants with (suspected) motility disorder: * (Part of) colon removed * Inflammatory bowel disease

Design outcomes

Primary

MeasureTime frameDescription
Power Percent DifferenceDuring EEnG procedureRelative power change when comparing pre-prandial EEnG measurements to post-prandial measurements. Power will be calculated as the mean amplitude (mV\^2/Hz) in a bandwidth of 2 cycles per minute around the dominant frequency related to colonic movements (between 2-10 cycles per minute).

Secondary

MeasureTime frameDescription
EEnG questionnaire scoreDirectly after EEnG procedure, which is a one time procedure the subjects in this study will undergoBurden score of EEnG procedure as assessed by a self created questionnaire (in collaboration with medical doctors, a psychologist and representatives of the patients association). A mean score of 0 indicates maximum burden, a mean score of 10 means no burden at all.
Gold Standard questionnaire scoreDirectly after EEnG procedure, which is a one time procedure the subjects in this study will undergo, or directly after the gold standard procedure, which some subjects will undergo in the near future at time of inclusionTotal burden score of Gold Standard procedure used to diagnose motility disorder as assessed by a self created questionnaire (in collaboration with medical doctors, a psychologist and representatives of the patients association). A mean score of 0 indicates maximum burden, a mean score of 10 means no burden at all.

Countries

Netherlands

Outcome results

None listed

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