A Study to Assess Defection Using MRI

Overview

About this study

The purpose of this study is to explain the mechanisms of impaired rectal evacuation characterizing phenotypes in functional defecation disorders, and ascertain if pelvic floor retraining can be tailored to underlying mechanisms.

 

Participation eligibility

Participant eligibility includes age, gender, type and stage of disease, and previous treatments or health concerns. Guidelines differ from study to study, and identify who can or cannot participate. There is no guarantee that every individual who qualifies and wants to participate in a trial will be enrolled. Contact the study team to discuss study eligibility and potential participation.

Inclusion Criteria- Healthy Controls:

  • Healthy female volunteers, aged 18-75 years.
  • Able to provide written informed consent before participating in the study.
  • Able to communicate adequately with the investigator and to comply with the requirements for the entire study.

Inclusion Criteria - Patients:

  • Females aged,18-75 years.
  • Having clinical features (i.e., symptoms and signs) of a functional defecation disorder.

Exclusion Criteria - Patients and Controls:

  • Clinical evidence (including physical exam and EKG) 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. 
  • Medications that may alter gastrointestinal motility; e.g., serotoninergic agents, alpha adrenergic agonists, calcium channel or b blockers; stable dose of thyroxine will be permitted.
  • Prior pelvic radiation or rectal resection, but not surgery for hemorrhoids or sigmoid resection.
  • History of panic attacks or claustrophobia during MRI.

Exclusion Criteria - Controls only:

  • Current symptoms of a functional gastrointestinal disorder assessed by questionnaire 15.
  • Putative risk factors for pelvic floor trauma; i.e., six or more vaginal deliveries, birthweight > 4500gms (macrosomia), or known 4th degree perineal tear.

Participating Mayo Clinic locations

Study statuses change often. Please contact the study team for the most up-to-date information regarding possible participation.

Mayo Clinic Location Status Contact

Rochester, Minn.

Mayo Clinic principal investigator

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

Closed for enrollment

Contact information:

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

(507) 255-2783

bharucha.adil@mayo.edu

More information

Publications

Publications are currently not available
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CLS-20506888

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