Evaluation of Gastrointestinal Symptoms and Quality of Life in Patients With Sphincter of Oddi Dysfunction

NCT01410071 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 153

Last updated 2011-08-04

No results posted yet for this study

Summary

The purpose of this research study is to see if there is a significant difference in improvement of symptoms and quality of life of those undergoing endoscopic therapy versus those wanting to control their symptoms with medicines or those who just want to wait and watch.

Conditions

Sponsors & Collaborators

  • Wake Forest University Health Sciences

    collaborator OTHER
  • Wisconsin Center for Advanced Research

    lead OTHER

Principal Investigators

  • Nalini M Guda, MD · GI Associates

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-09-30
Primary Completion
2009-06-30
Completion
2009-08-31

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01410071 on ClinicalTrials.gov