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Use of an Ambulatory Capsule to Characterize Gastrointestinal Pressure Patterns in Children

NCT01026922 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 22

Last updated 2018-07-19

No results posted yet for this study

Summary

This study will test a new medical device called the SmartPill GI Monitoring System, which is now used to diagnose gastric motility disorders in adults, in children. The study will compare the SmartPill capsule findings to antroduodenal manometry (ADM), which is a standard procedure currently used for the evaluation of gastric and duodenal motility in children. The ADM studies will be done for clinical purposes and only if recommended by the patient's gastroenterologist. The research portion of the study is limited to the use of SmartPill.

Conditions

  • Upper Gastrointestinal Motility Disorders

Sponsors & Collaborators

  • The SmartPill Corporation

    collaborator INDUSTRY

  • Nationwide Children's Hospital

    lead OTHER

Principal Investigators

  • Carlo Di Lorenzo, MD · Nationwide Children's Hospital

Eligibility

Min Age
10 Years
Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-12-31
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • United States

Study Locations

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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 NCT01026922 on ClinicalTrials.gov