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Investigating the effect of a new wound dressing containing alginate salts and silver particles for diabetic wound healing

Clinical studies on wound dressings containing alginate salts and silver particles for diabetic wound healing

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240703062321N2
Enrollment
25
Registered
2026-05-19
Start date
2026-05-30
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetic wounds. Type 2 diabetes mellitus with foot ulcer

Interventions

Intervention 1: Intervention Group: Use of a wound dressing containing alginate salts and silver particles.First, the wound bed must be prepared. To begin, wash hands and put on sterile gloves. Clean
the hydrogel surface must be in full contact with the moist wound bed.Place the alginate hydrogel film directly onto the wound bed. Upon contact with wound exudate, the alginate reacts with calcium io

Sponsors

Tehran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: Diabetic patients with chronic wounds who meet the following criteria Age 18 to 75 years Diagnosis of type 1 or 2 diabetes Diabetic wound in the slow or chronic healing phase Signed informed consent

Exclusion criteria

Exclusion criteria: Diabetic wounds with active infectious diseases Use of topical or systemic treatments that may affect wound healing

Design outcomes

Primary

MeasureTime frame
Percentage of wound area. Timepoint: Days 7, 14, 21, 28 (and then monthly if needed until complete recovery or up to 12 weeks). Method of measurement: Measurement of wound dimensions at each follow-up session.

Secondary

MeasureTime frame
Granulation tissue formation. Timepoint: Days 7, 14, 21, 28 (and then monthly if needed until complete recovery or up to 12 weeks). Method of measurement: observational.;Epithelium formation. Timepoint: Days 7, 14, 21, 28 (and then monthly if needed until complete recovery or up to 12 weeks). Method of measurement: observational.;Bacterial load. Timepoint: Days 7, 14, 21, 28 (and then monthly if needed until complete recovery or up to 12 weeks). Method of measurement: Microbial culture.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mahnaz Khanavi

Tehran University of Medical Sciences

khanavim@tums.ac.ir+98 21 4293 3261

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Jun 11, 2026