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Early Post-operative Monitoring by Sensor of Patients Undergoing Forefoot Surgery

NCT06242002 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2025-02-13

No results posted yet for this study

Summary

The goal of this clinical trial is to evaluate the monitoring using a sensor in patients who have undergone forefoot surgery, during the first 7 post-operative days.

The monitoring tool has a Global Positioning System (GPS) beacon, a 3-axis accelerometer and a temperature sensor, as well as an "emergency call" button.

The main objective it aims to answer are:

* to evaluate the feasibility of post-operative monitoring using this tool
* to evaluate the reliability of the tool

The investigators hope to determine if using this tool can be able to provide patients a "connected" personalized real-time monitoring for follow-up.

Conditions

  • Foot Injury

Interventions

PROCEDURE

Set up of sensor

Surgery is performed as usual for patients needing this medical procedure. At the end, the sensor is set up under the surgical dressing.

Sponsors & Collaborators

  • Clinique de lEurope a Amiens

    lead OTHER_GOV

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-01-19
Primary Completion
2024-12-31
Completion
2025-01-31

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06242002 on ClinicalTrials.gov