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Impact of Ostom-i Alert Sensor on Quality of Life in Patients With Ileostomy

NCT02472639 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 7

Last updated 2017-11-09

Study results available
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Summary

The purpose of this study is to evaluate patient satisfaction and quality of life in patients with ileostomy managed with or without the novel Ostom-i Alert device.

Conditions

  • Ostomy

Interventions

DEVICE

Ostom-i Alert Sensor

Wear the Ostom-i Alert Sensor

OTHER

No Ostom-i Alert Sensor

Patient will not use device

Sponsors & Collaborators

  • Cedars-Sinai Medical Center

    lead OTHER

Principal Investigators

  • Karen Zaghiyan, MD · Cedars-Sinai Medical Center

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-06-10
Primary Completion
2016-05-26
Completion
2016-05-26

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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 NCT02472639 on ClinicalTrials.gov