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NCT02694757

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

Terminated NA Results posted Last updated 19 March 2020
What this trial tests

NA trial testing Ostom-i device in Ileostomy - Stoma in 3 participants. Terminated before completion.

Timeline
1 August 2017
Primary endpoint
4 March 2019
4 March 2019

Quick facts

Lead sponsorMassachusetts General Hospital
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment3
Start date1 August 2017
Primary completion4 March 2019
Estimated completion4 March 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Massachusetts General Hospital

Who can join

18 and older, any sex, with Ileostomy - Stoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Ileostomy - Stoma

Currently open trials in the same condition.

Other Massachusetts General Hospital trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT02694757.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing