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.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 30 (estimated) |
| Sponsor | ABIGO Medical AB Industry-sponsored |
| Locations | 1 site (Mölndal) |
| Status | Recruiting |
| Started | April 5, 2025 |
| Main results expected | December 2026 |
| Study ends | December 2026 |
| Registry record updated | September 14, 2026 |
| Trial ID | NCT05089890 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
- Principal investigator: Anders Jönsson, MD — Sahlgrenska University Hospital
- Study coordinator: Fana Hunegnaw
- Email: fana.hunegnaw@essity.com
- Phone: +46761361512
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.