Ostom-i Alert Sensor Quality of Life Validation

Trial ID or NCT#

NCT02319434

Status

Purpose

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.

Official Title

Validating the Use of a Novel Wearable Device in Improving Quality of Life of Ostomy Patients

Eligibility Criteria

Ages Eligible for Study: 18 Years to 80 Years
Sexes Eligible for Study: All
Accepts Healthy Volunteers: No
Inclusion Criteria:
  1. - 18-80 years of age - use of an ostomy bag for at least six months - must own an iPhone, iPod Touch, or Android
Exclusion Criteria:
  1. - use of large urostomy bags
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Investigator(s)

Lawrence Chu, MD, MS
Lawrence Chu, MD, MS
Anesthesiologist
Professor of Anesthesiology, Perioperative and Pain Medicine

Contact us to find out if this trial is right for you.

Contact

Dara Rouholiman, BS
6507236632

View on ClinicalTrials.gov