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Comparison of Agicoat and Vaseline Gauze dressing

Comparison of Agicoat and Vaseline Gauze dressing on time of repair on Split-thickness skin graft donor sites

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220917055975N1
Enrollment
17
Registered
2022-11-01
Start date
2022-02-28
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Split-thickness skin graft donor sites. Skin donor, autologous

Interventions

Intervention 1: Intervention 1: Coverage of the skin graft donor site with agicoat dressing. The dressing will not be disturbed till 4th post operative day and then will be changed every 4 days, till

Sponsors

Gorgan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: no comorbidities, no medication aged between 18 and 70years planned toundergo Split-Thickness Skin Graft harvest from the thighs orbuttocks Patients sign informed consent form

Exclusion criteria

Exclusion criteria: Coagulative diseases Patients with an immunocompromised state Pregnancy/Lactation Hypersensitivity to dressing components Chemical or electrical burns Patients with burns whose analgesic requirement were more and difficult to compare with the study proposed Mentally-ill patients and any condition which influences pain recording Local infection at planned split-thickness skin graft donor site Comorbidities that may affect wound healing Burn site>30% of body surface area Brevious skin graft from the same donor site

Design outcomes

Primary

MeasureTime frame
Healing time(Defined as time elapsed between split thickness skin graft harvest and complete donor-site reepithelialization). Timepoint: Examination on 4, 8 days and weekly until the dressing is completely removed? after surgery. Method of measurement: Examination? Metric Grid Tracing.

Secondary

MeasureTime frame
Pain(An unpleasant sensation associated with tissue damage). Timepoint: Four and eight days after surgery. Method of measurement: Visual analogue scale(VAS).;Scar durability(The final result of the surgical site). Timepoint: Three and six months after beginning of intervention. Method of measurement: Vancouver scar scale (VSS).;Infection: Defined as the presence of replicating microorganisms within a wound leading. Timepoint: Before the intervention, If necessary, on 4, 8 days after surgery. Method of measurement: Examination, Wound Culture.;Percentage of epithelialization(The amount of wound healing was recorded based on the percentage of epithelialization). Timepoint: Four and eight days after surgery. Method of measurement: Metric grid tracing(Calculation of the ratio of the surface area of the epithelialized parts to the total surface area of the donor site).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactValiollah Alishahi

Gorgan University of Medical Sciences

valiollahalishahi@gmail.com+98 17 3222 0561

Outcome results

None listed

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