Trial to Understand Efficacy of Colesevelam in Diarrhea Predominant IBS Patients With Bile Acid Malabsorption

Overview

Información sobre este estudio

To compare with a randomized trial (n=15 per treatment group), effects of colesevelam and placebo treatment, on colonic transit, bowel functions, permeability and tight junction expression in rectosigmoid mucosa of IBS-D with Bile Acid Malabsorption.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

Inclusion Criteria:

  • Females and males age 18 -75 with a positive diagnosis of IBS based on the Rome III criteria. This criteria is: a diagnosis for at least 3 months, with onset at least 6 months previously, of recurrent abdominal pain or discomfort associated with 2 or more of the following:
    1. Improvement with defecation; and/or
    2. Onset associated with a change in frequency of stool; and/or
    3. Onset associated with a change in form (appearance) of stool (discomfort means an uncomfortable sensation not described as pain). BAM serum alpha C4 ≥ 40 ng/mL or FGF19 ≤ 80 pg/mL or fecal BA >2000 µmoles/48h.
  •  Total fecal BA > 1000 µmoles/48h + >4% primary BA, or >10% primary BA

Exclusion Criteria:

Patients diagnosed with IBS with known clinically-relevant inflammation bleeding diathesis will be excluded, given the need for sigmoid mucosal biopsies. Patients participating will not take any of the following disallowed medications for at least 7 days prior to and during the remainder of the study:

  1. Any treatment specifically taken for IBS-D, including loperamide, cholestyramine, alosetron
  2. Drugs with a known pharmacological activity at 5-HT4, 5-HT2b or 5-HT3 receptors (e.g, tegaserod, ondansetron, tropisetron, granisetron, dolasetron, mirtazepine, cilansetron);
  3. All narcotics (e.g, codeine, morphine, and propoxyphene, either alone or in combination)
  4. Anti-cholinergic agents (e.g, dicyclomine, hyoscyamine, propantheline).
  5. Tramadol
  6. GI preparations:
    • Anti-nausea agents (e.g, trimethobenzamide, promethazine, prochlorperazine, dimenhydrinate, hydroxyzine);
    • Osmotic laxative agents (e.g, lactulose, sorbitol or PEG solutions as Miralax and Glycolax);
    • Prokinetic agents (e.g, cisapride, metoclopramide, prucalopride, domperidone);
    • 5-HT3 antagonists (e.g. alosetron)
  7. Oral anticoagulants
  8. Antimuscarinics
  9. Peppermint oil
  10. Systemic antibiotics, as well as antibiotics directed at colonic flora such as rifaximin and metronidazole

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus

Rochester, Minn.

Investigador principal de Mayo Clinic

Michael Camilleri, M.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
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CLS-20344119

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