The effect of hydrocolloid dressing in the treatment of skin graft wounds

Evaluation of the effectiveness of silver-containing hydrocolloid dressings in the treatment of donor wounds of partial- thickness skin grafts

Status

Active, not recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20220302054168N1

Enrollment

Registered

2022-03-03

Start date

2022-03-21

Completion date

Unknown

Last updated

2022-03-08

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

Conditions

Patients with skin defects. Other early skin lesions of yaws

Interventions

Intervention 1: Intervention group: First, the partial- thickness skin grafts removed with an electric dermatome.The location of the donor, the thickness of the skin removed, and the dimensions of the

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who need partial partial- thickness skin grafts to repair skin defects for various reasons

Exclusion criteria

Exclusion criteria: Patients who do not wish to participate in the study Patients with previously known allergies to silver

Design outcomes

Primary

Measure	Time frame
The degree of adhesion of the dressing to the wound bed. Timepoint: After dressing the wound up to 14 days after dressing. Method of measurement: Standard checklist.;Wound infection. Timepoint: After dressing the wound up to 14 days after dressing. Method of measurement: Standard checklist.	—

Secondary

Measure	Time frame
Wound healing process. Timepoint: After dressing the wound up to 14 days after dressing. Method of measurement: Standard checklist.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAmirAli Mirfakhraei

Iran University of Medical Sciences

Dr.mirfakhraee@gmail.com+98 21 8871 7272

Outcome results

None listed

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