Efficacy of Ostom-i Alert System at Decreasing Dehydration Related Complications

Stopped early · Not applicable

Conditions studied: Ileostomy - Stoma

In brief

The purpose of this study is to evaluate the efficacy of the Ostom-i device in decreasing readmission rates of subjects with new ileostomies in the first 30 days post-operatively.

Key facts

Study ID

NCT02694757

Run by

Massachusetts General Hospital

People needed

3

Starts

2017-08-01

Expected to finish

2019-03-04

Last updated by the study team

2020-03-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• >18 years of age
• English speaking
• creation of new ileostomy
• access to smartphone with bluetooth technology to support OIA application
• able to give written consent
• have preoperative counseling about stoma with ostomy nurse (excludes emergent ostomy creation)

Where it is running

• Massachusetts General Hospital — Boston, Massachusetts, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.