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Amniotic membrane extract drops in wound healing of semi-thickness skin donor site

Phase 2
Recruiting
Conditions
Wound.
Open wound of unspecified body region
Registration Number
IRCT201703148177N16
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
46
Inclusion Criteria

age 18-65 years old; requiring skin graft surgery; signing informed consent. Exclusion criteria: removal of skin graft from the outside of the thigh; conditions and diseases in which the immune system is weakened and wound healing is delayed such as: diabetes, cancer, immune system dysfunction, drugs that suppress the immune system, taking corticosteroids, smoking and alcohol; patients who do not cooperate with treatment and referrals necessary after surgery.

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Wound Healing. Timepoint: Observation, examination and photography on days 1 and 12 after surgery and during spontaneous separation of Vaseline gauze from wound. Method of measurement: Observation, examination and photography.
Secondary Outcome Measures
NameTimeMethod
Cost. Timepoint: The end of the study. Method of measurement: Cost estimation of the number of drops used in each treatment group.;Scar. Timepoint: 6 months after surgery. Method of measurement: Vancouver Scar Scale, Patient and Observer Scar Assessment Scale (POSAS).;Infection. Timepoint: Every 3 days after surgery until complete wound healing. Method of measurement: Observation, examination and wound culture.;Pain. Timepoint: 3, 6 and 12 days after surgery. Method of measurement: Visual Analogue Scale (VAS).
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