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Comparison of the effect of nanosilver spray (Silvosept) and silver particles spray containing chitosanand sodium alginate (Revahealsept) in the management of diabetic wounds: a randomized clinical trial

Comparison of the effect of nanosilver spray (Silvosept) and silver particles spray containing chitosanand sodium alginate (Revahealsept) in the management of diabetic wounds: a randomized clinical trial

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20250119064437N1
Enrollment
60
Registered
2025-04-04
Start date
2025-03-10
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Condition 1: Diabetic wound in a patient with diabetes. Condition 2: Diabetic wound in a patient with diabetes. Type 2 diabetes mellitus with foot ulcer Type 1 diabetes mellitus with foot ulcer

Interventions

Intervention 1: Intervention group: For this group of patients, simple alginate dressings, absorbent pads, and Rawahil Sept spray, a product of Rasa Salamat Arvand Company, will be used. Intervention

Sponsors

Karaj University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Have a diabetic foot ulcer in stage 1 to 2 on the Wagner scale The size of their wounds should be less than 10 x 10 centimeters Have a voluntary interest in participating in the project Have adequate arterial perfusion

Exclusion criteria

Exclusion criteria: Patient's unwillingness to participate in the study The patient's unwillingness to continue the study No referral for any follow-up to assess the outcome of treatment In case of limb amputation In case of patient sensitivity to any of the components of the spray under study

Design outcomes

Primary

MeasureTime frame
The rate of reduction in the degree of wound. Timepoint: The first, seventh, fourteenth, twenty-first days, ... up to two months after the dressing is applied or the dressing is completed for any reason, including recovery or patient referral. Method of measurement: In all cases, the wound will be debrided and after debridement, the depth and area of ??the wound will be measured by the researcher with a disposable graduated ruler and the wound will be photographed with a digital camera to document it. To ensure uniformity, all photographs will be taken at a distance of 30 cm and from a frontal angle. A graduated ruler will be used near the wound when photographing the wound.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactYasaman Firouzi Etminan

Karaj University of Medical Sciences

yasamanfirouzietminan@gmail.com+98 26 3455 2001

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026