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

comparison of short-term outcomes between amniotic membrane and conventional dressing in skin graft Donor site in patients hospitalized in the burn ward of Imam Khomeini Hospital of Urmia in 2019

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190614043889N1
Enrollment
26
Registered
2020-02-13
Start date
2019-06-04
Completion date
Unknown
Last updated
2020-02-24

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

Conditions

Burn. Donor Graft Side. Burn of unspecified body region, unspecified degree

Interventions

Intervention 1: Intervention group: the patient's left side will be dressed biologically with amniotic membrane. Intervention 2: Control group:The right side of the patient is dressed with Nitrofurazo

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
1 Years to 66 Years

Inclusion criteria

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

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
Local 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).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJafar Kazemzadeh

Oroumia University of Medical Sciences

jafar.kazemzade48@gmail.com+98 44 3198 8111

Outcome results

None listed

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