Actively Recruiting

Age: 18Years +
All Genders
NCT06321978

Mepilex Border Flex Utilization Pilot Spain

Led by Molnlycke Health Care AB · Updated on 2024-05-23

40

Participants Needed

1

Research Sites

15 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The aim of this study is to assess and describe the utilization of Mepilex® Border Flex and other foam dressings available in routine clinical practice in the management of patients with chronic wounds, in order to understand the pattern of use and the frequency of dressing changes in wound management. The study will also allow to gain information about the opinion of the HCPs and the patient's experience concerning wound management with foam dressings. This information may help to understand patient's health care optimization in terms of quality and efficiency.

CONDITIONS

Official Title

Mepilex Border Flex Utilization Pilot Spain

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 18 years or older.
  • The patient has been deemed by the HCP to change dressing to Mepilex® Border Flex.
  • Patients with chronic wounds (wounds that have not reduced in size by more than 40% to 50% or healed within a month) treated with foam dressings, other that Mepilex® Border Flex, according to its intended use at baseline visit for minimum 4 weeks.
  • Patients with an expectation of wound follow-up of at least 4 weeks.
  • Patients agree only to have the dressing changed by the HCP.
  • Patients capable of signing the Informed Consent Form and answer the questions being asked.
Not Eligible

You will not qualify if you...

  • Patients with any applicable contraindication or sensibilization to any of the dressing compounds
  • Patients with pressure ulcers (PU) stage I, deep tissue injuries or terminal wounds (e.g., fungating wounds)
  • Patients with wounds whose location and/or aetiology requires a dressing change for reasons that are unrelated to the dressing characteristics such as wounds in the sacral area.
  • Hospice patients
  • Patients participating in other studies interfering with this study.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

CS Ciudad Expo - Mairena de Aljarafe

Seville, Andalusia, Spain, 41927

Actively Recruiting

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Research Team

F

Fia Navntoft

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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