Clinical trial Recruiting at 1 site Interventional Ages 18 and up

Sorbact dressings in hard-to-heal wounds

Official title: An Open, Single-centre, Clinical Investigation to Explore the Binding of Bacteria and Fungi to Dialkylcarbamoyl Chloride (DACC)-Coated Dressings From Hard-to-heal Wounds

Run by ABIGO Medical AB · NCT05089890 · Data updated 2026-11-12

This study tests whether Sorbact dressings can bind bacteria and fungi from hard-to-heal wounds in adults.

More Diabetic Foot Ulcer trials

Quick facts

Study typeInterventional
Ages18 Years and up
SexAll
Enrollment30 (estimated)
SponsorABIGO Medical AB
Industry-sponsored
Locations1 site (Mölndal)
StatusRecruiting
StartedApril 5, 2025
Main results expectedDecember 2026
Study endsDecember 2026
Registry record updatedSeptember 14, 2026
Trial IDNCT05089890 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18+) with a hard-to-heal wound for at least 6 weeks and starting one of the Sorbact dressings.

Probably not a fit

Patients whose wounds do not respond to the dressing or who do not experience reduced bioburden may not see a benefit.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is an open, single-center, exploratory study to see if three Sorbact dressings can bind bacteria and fungi from hard-to-heal wounds over 14 days. Participants are adults with hard-to-heal wounds starting one of the Sorbact dressings, assigned to Compress, Gel Dressing, or Ribbon Gauze in groups of 10. The study includes three visits (screening/baseline and two follow-ups) at Sahlgrenska University Hospital in Sweden. Outcomes focus on the extent of microbial binding to the dressing surface under real-use conditions.

Why it matters

Potential benefit: If successful, the dressings may help reduce wound bioburden and support healing in hard-to-heal wounds.

How similar studies have gone: Previous Sorbact studies have shown binding of microbes to its dressings in similar settings, supporting this exploratory approach.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

1. Able to read and understand the Subject Information and Informed Consent Form and provide meaningful informed consent
2. Due to start using one of the following dressings: Sorbact® Compress, Sorbact® Gel Dressing and Sorbact® Ribbon Gauze
3. Age ≥18 years
4. Presence of hard-to-heal wound for ≥6 weeks with no significant wound area reduction for the last 4 weeks confirmed by investigator/study nurse

Exclusion Criteria:

1. Participating in another clinical investigation
2. Known allergy or sensitivity to any components of the allocated investigational device
3. Use of antimicrobial agent (e.g., silver- or iodine-containing dressings, or gels) during the last wo weeks
4. Use of a dressing from the Sorbact® range during the last two weeks
5. Subjects with any other condition that as judged by the investigator may make investigation procedures inappropriate

Where it's running

  • Sahlgrenska University Hospital
    Mölndal, Sweden
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.