Comparison of between amniotic membrane and conventional dressing outcomes in burned skin graft Donor site

Not Applicable

• Conditions: Burn. Donor Graft Side.; Burn of unspecified body region, unspecified degree; T30.0

• Registration Number: IRCT20190614043889N1
• Lead Sponsor: Oroumia University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 24 February 2020

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 26

Inclusion Criteria

patient age 1-66 years old
Patient accept biologic dressing
Burns require skin grafts regardless of burning percent

Exclusion Criteria

have underlying disease such as diabetes mellitus renal failure hepatitis vascular in sufficiency and heart disease
patient have other trauma

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Epithelialization and scar in donor graft site. Timepoint: effect of Biologic dressing in donor graft site on days 7, 14 and 30. Method of measurement: Information Gathering Form.

Secondary Outcome Measures

Name	Time	Method
ocal infection rate. Timepoint: over a period of one month. Method of measurement: observed local infection.;Amount of pain. Timepoint: during a period of one month. Method of measurement: Visual Analogue Scale.;Patients' rate of co-operation in dressing replacement. Timepoint: during a period of one month. Method of measurement: observation.;Duration of recovery time. Timepoint: over a period of one month. Method of measurement: week.;Itching rate. Timepoint: during a period of one month. Method of measurement: to measure with Nominal Scale (yes/no).