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NCT05579743 · ClinicalTrials.gov registry record · NA

Feasibility and Effectiveness of a Remote Monitoring Program for the Treatment of Diabetic Foot Ulcers

A NA study of Diabetic Foot Ulcer and Diabetic Foot, sponsored by Johns Hopkins University.

Recruiting
Registry status
NA
Development phase
120
Enrollment target
1
Study location

NCT05579743 is a NA study of Diabetic Foot Ulcer and Diabetic Foot that is actively recruiting participants, run by Johns Hopkins University. The registered enrollment target is 120 participants, below the 253-participant average among 67 other Diabetic Foot Ulcer trials with a reported enrollment target (53% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05579743, a NA study of Diabetic Foot Ulcer and Diabetic Foot, is actively recruiting participants, sponsored by Johns Hopkins University.

RECRUITING
Registry status
NA
Development phase
120 participants
Enrollment target
1
Study location

Study Summary

This research is being done to compare two different methods of wound monitoring for chronic wounds: remote wound monitoring using a smartphone app and in-person wound monitoring in a clinic setting. This will be a pilot non-blinded randomized controlled feasibility trial. The investigators will enroll 120 patients with an active diabetic foot ulcer (DFU) who present to the multidisciplinary diabetic foot clinic in Baltimore, Maryland. Patients will be computer randomized 1:1 to receive wound care monitoring using remote DFU monitoring technology or standard in-person monitoring for 12 weeks.

Interventions

  • OTHER Remote wound monitoring technology

Study Locations (1)

Maryland

  • Johns Hopkins University School of Medicine - Baltimore

Trial Details

FieldValue
Enrollment Target 120 participants
Start Date 2023-01-06
Est. Completion 2026-03-30
Phase NA

Sponsor

Johns Hopkins University

1,448 total trials

What the Registry Record Tells You About NCT05579743

The ClinicalTrials.gov registry entry for NCT05579743 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 120 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 253-participant average among 67 other Diabetic Foot Ulcer trials with a reported enrollment target (53% lower). The listed sponsor is Johns Hopkins University, which has 1,448 total studies on file at ClinicalTrials.gov.

The record links to 6 conditions, with Diabetic Foot Ulcer appearing as the primary indexed condition, and to 1 intervention - of which Remote wound monitoring technology is the first listed.

NCT05579743 reports 1 study location spanning 1 distinct geographic area - top geographies include Maryland.

Frequently Asked Questions

What is clinical trial NCT05579743 about?

NCT05579743 is a clinical study titled "Feasibility and Effectiveness of a Remote Monitoring Program for the Treatment of Diabetic Foot Ulcers". This research is being done to compare two different methods of wound monitoring for chronic wounds: remote wound monitoring using a smartphone app and in-person wound monitoring in a clinic setting. This will be a pilot non-blinded randomized controlled feasibility trial. The investigators will enr...

What is the current status of trial NCT05579743?

This trial is currently recruiting. It is a NA study. The enrollment target is 120 participants. The study started on 2023-01-06. Estimated completion is 2026-03-30.

What conditions does trial NCT05579743 study?

This clinical trial studies the following conditions: Diabetic Foot Ulcer, Diabetic Foot, Wound Heal, Diabetes Complications, Wound; Foot.

What interventions are being tested in trial NCT05579743?

The interventions under investigation include: Remote wound monitoring technology (OTHER).

Who is sponsoring clinical trial NCT05579743?

This trial is sponsored by Johns Hopkins University, which has 1,448 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05579743 being conducted?

This trial has 1 study location across Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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