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Ostom-i Alert Sensor Quality of Life Validation

NCT02319434 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 20

Last updated 2018-12-07

No results posted yet for this study

Summary

The purpose of this study is to determine the usability and acceptance of the Ostom-i Alert Sensor. The investigators would like to see if is generally helpful to ostomy patients and whether it has a beneficial impact on living with an ostomy bag. Results from this study will be used to determine if a larger clinical study is feasible.

Conditions

  • Ostomy

Interventions

DEVICE

Ostom-i Alert Sensor

Sensor on ostomy bag.

Sponsors & Collaborators

Principal Investigators

  • Larry F Chu, MD · Stanford School of Medicine

Eligibility

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

Timeline & Regulatory

Start
2015-11-30
Primary Completion
2019-03-01
Completion
2019-03-01

Countries

  • United States

Study Locations

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Entities

Companies

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 NCT02319434 on ClinicalTrials.gov