An Investigation to Identify Subjects Admitted to Hospital With an Increased Risk of Developing Pressure Ulcers

NCT05458050 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 433

Last updated 2023-08-25

No results posted yet for this study

Summary

A double blind, non randomized, multicenter investigation

Conditions

  • Pressure Ulcer

Interventions

DEVICE

PU sensor

Device to assess microcirculation in sacrum area to find subjects at risk for pressure ulcer

Sponsors & Collaborators

  • Aurevia

    collaborator INDUSTRY
  • PU sensor AB

    lead INDUSTRY

Principal Investigators

  • Anna-Christina Ek, RN,PhD · PU Sensor

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-01
Primary Completion
2023-06-30
Completion
2023-08-24

Countries

  • Sweden

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 NCT05458050 on ClinicalTrials.gov