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Study identifier: NCT06300762 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

RCT Exudate Management Cutimed Sorbion Product Range

Condition: Venous Leg Ulcer  ·  Sponsor: BSN Medical GmbH

PhaseNA
Planned participants152
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The fluid handling capacity of superabsorbent dressings varies depending on the design and construction. The use of effective advanced wound dressings is a promising strategy to achieve adequate absorption of wound exudate and malodour promoting wound healing. The aim of the current study is to determine whether there is a difference in the clinical performance of exudate absorption with two commonly used CE-marked superabsorbent dressings when used on VLUs in routine wound care. As primary objective the dressing´s absorption performance and its ability to prevent skin maceration and leakage of the wound dressing will be investigated.

This description comes directly from the study's public registry record.

Talk to the study team

Hardy Schweigel, PhD  ·  +491522  ·  hardy.schweigel@essity.com

Sandra Tobisch  ·  sandra.tobisch@essity.com

Always discuss trial participation with your own doctor first.

Locations (3)

Niels Stensen Klinik, Christliches-Klinikum-MelleMelle, Niedersachsten, GermanyRecruiting
Mid Yorkshire Teaching NHS Trust Pinderfields HospitalWakefield, West Yorkshire, United KingdomRecruiting
Northumbria Healthcare NHS Foundation TrustAshington, United KingdomRecruiting

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Source record: clinicaltrials.gov/study/NCT06300762