Status:

COMPLETED

Validation of the Small Intestine Microbiome Aspiration (SIMBA) Capsule

Lead Sponsor:

University of Calgary

Collaborating Sponsors:

Nimble Science Ltd.

Conditions:

Proof of Concept

Irritable Bowel Syndrome

Eligibility:

All Genders

18-70 years

Phase:

NA

Brief Summary

Prospective, open label trial to establish the ability of the SIMBA Capsule to accurately obtain a sample from the small bowel of participants with IBS (10 constipation-predominant (IBS-C) and 10 diar...

Eligibility Criteria

Inclusion

  • Inclusion Criteria
  • Aged between 18 and 70 years.
  • Diagnosis of IBS by Rome 4 criteria (IBS groups) or no previous diagnosis of IBS or suspected IBS (Control group).
  • Ability to understand and provide informed consent.
  • Ability and willingness to meet the required schedule and study interventions.
  • No planned change in diet or medical interventions during the study duration.
  • Adequate mobility to transfer repeatedly between X-ray (standing or lying), and waiting (sitting).
  • Willing and able to undergo a sedated esophagogastroduodenoscopy (EGD) with aspirate and brushing.
  • Exclusion Criteria
  • Prior gastrointestinal disease, surgery, or radiation treatment which, in the investigator's opinion, would lead to intestinal structuring or obstruction with a risk of capsule non-excretion (particular diseases which would be assessed on a case-by-case basis would include, achalasia, eosinophilic esophagitis, Crohn's disease, cancer diagnosis or treatment within the past year, or previous esophageal, gastric, small intestinal, or colonic surgery. Appendectomy or cholecystectomy more than 3 months prior to enrollment are acceptable).
  • Use of any medications in the previous week that could substantially alter gastrointestinal motor function (e.g., opioids, prokinetics, anticholinergics, laxatives), or acidity (PPI, H2RA).
  • History of oropharyngeal dysphagia or other swallowing disorder with a risk of aspiration of the capsule.
  • Females of childbearing age who are not practicing birth control and/or are pregnant or lactating.
  • No antibiotics, or colon cleanses/bowel prep for 2 weeks.
  • \< 2 bowel movements per week (Control Group).

Exclusion

    Key Trial Info

    Start Date :

    October 27 2021

    Trial Type :

    INTERVENTIONAL

    Allocation :

    ACTUAL

    End Date :

    June 16 2022

    Estimated Enrollment :

    30 Patients enrolled

    Trial Details

    Trial ID

    NCT04094558

    Start Date

    October 27 2021

    End Date

    June 16 2022

    Last Update

    September 2 2022

    Active Locations (1)

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    Cumming School of Medicine, University of Calgary

    Calgary, Alberta, Canada, T2N 4Z6