Foam Dressing for Chronic Venous Leg Ulcers

A Clinical Investigation to Follow the Progress of Exuding Chronic Venous Leg Ulcers Using a Non-Bordered Foam Dressing

Recruiting N/A Interventional Study
Wounds Wound of Skin Wound Leg Venous Leg Ulcer
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
20 (estimated)
Sponsor
Molnlycke Health Care AB · Industry
Who this trial is looking for

This trial is looking for adults with chronic venous leg ulcers. Participants will wear a special foam dressing for up to 6 weeks while their wounds are monitored.

Are You a Good Fit for This Trial?

You may be able to join if

  • I am an adult aged 18 or older.
  • I have been diagnosed with a chronic, exuding venous leg ulcer.
  • My ulcer has a moderate to large amount of fluid.
  • My wound size is between 3 cm2 and 30 cm2.
  • I consent to participate and allow digital imaging of my wound.
  • I will comply with compression therapy.

You may not be able to join if

  • I have an infected ulcer that needs antibiotics.
  • I have a circumferential wound.
  • I am allergic to the materials in the dressing.
  • I am using wound fillers.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer three quick questions written from this study's own rules to see if you may qualify. No account needed to find out.

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About This Trial

The goal of this clinical trial to follow the progress of wounds in those with chronic venous leg ulcers while using a non-bordered foam dressing. The main objective is to follow the progress of these wounds over time from initial visit to each follow-up visit. Participants will be asked to wear the dressing for up to 6 weeks of treatment or until healed, changed at every one-week interval.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Signed consent to participate (including consent for digital imaging) * Adult aged ≥18 years * Diagnosed with a chronic, exuding VLU * Exudate amount moderate to large * Wound size from 3 cm2 to 30 cm2, as determined by the clinician * ABPI (within 3 months) \> 0.7. If ABPI \>…
Contacts

Janet Kandrevas, MD, MS

734-358-2174

janet.kandrevas@molnlycke.com

CONTACT

Andrea Picchietti, MS, CCRA

260-258-3879

andrea.picchietti@molnlycke.com

CONTACT