A Study to Assess Anal Pressures by Manometry in Health People

Overview

Información sobre este estudio

The specific aims of this study are to measure recto-anal pressures measured by portable manometry at rest, during squeeze, during simulated evacuation, rectal distention, and during a Valsalva maneuver in asymptomatic healthy women and men.

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

  1. Do not meet symptom-based criteria for constipation, fecal incontinence or irritable bowel syndrome by validated questionnaires
  2. Able to provide written informed consent before participating in the study
  3. Able to communicate adequately with the investigator and to comply with the requirements for the entire study.

Exclusion Criteria

  1. BMI ≥ 30 kg/m²
  2. Clinical evidence of significant cardiovascular, respiratory, renal, hepatic, gastrointestinal, hematological, neurological, psychiatric or other disease that may interfere with the objectives of the study and/or pose safety concerns.
  3. During digital rectal examination, markedly reduced anal contractile response or perineal descent during simulated evacuation.
  4. Medications that may alter gastrointestinal motility, e.g., serotoninergic agents, alpha adrenergic agonists or antagonists, calcium channel blockers or opiates.
  5. Prior pelvic radiation; history of or current inflammatory bowel disease
  6. Putative risk factors for pelvic floor trauma, i.e. > 4 vaginal deliveries, known birthweight >4500 gms (Macrosomia), known 4th degree perineal tear, or known forceps use.
  7. Any anorectal procedures (including for hemorrhoids)

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

Adil Bharucha, M.B.B.S., M.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
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CLS-20402163

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