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NCT06053047: MASTER

Remote Monitoring of the Diabetic Foot to Prevent Re-Ulceration

Terminated NA Last updated 17 October 2024
What this trial tests

NA trial testing Bluedrop Monitoring Service (BMS) in Diabetic Foot in 26 participants. Terminated before completion.

Timeline
22 January 2024
Primary endpoint
18 September 2024
18 September 2024

Quick facts

Lead sponsorBluedrop Medical Limited
PhaseNA
StatusTerminated
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingnone
Primary purposeprevention
Enrollment26
Start date22 January 2024
Primary completion18 September 2024
Estimated completion18 September 2024
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Bluedrop Medical Limited

Who can join

18 and older, any sex, with Diabetic Foot. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to understand the effects of the Bluedrop Monitoring System (BMS) on the development of diabetic foot ulcers. All Participants in this study will continue with their normal foot care and complete surveys with questions about their foot health every three months. Participants selected to receive the Bluedrop Monitoring System (BMS) will place it in their home and stand on it once a day for 12 months. Participants will also need to answer questions about their general foot health and, if using the system, their experience using the device and monitoring service.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Diabetic Foot

Currently open trials in the same condition.

Other Bluedrop Medical Limited 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/NCT06053047.

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