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Comparison of dressing of 1% silver sulfadiazine cream with combination of 10% Betadine and 1% Acetic Acid in the management of Deep Partial-Thickness (Deep Second-Degree) Burn Wounds

Comparison of dressing of 1% silver sulfadiazine cream with combination of 10% Betadine and 1% Acetic Acid in the management of Deep Partial-Thickness (Deep Second-Degree) Burn Wounds

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171023036962N1
Enrollment
60
Registered
2018-05-04
Start date
2017-09-23
Completion date
Unknown
Last updated
2018-06-18

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

Conditions

management of Deep Partial-Thickness (Deep Second-Degree) Burn Wounds. Burn of second degree, body region unspecified

Interventions

Intervention 1: Intervention group: After wound washing, they are daily dressed with silver sulfadiazine 1% cream (1.5 mm thick on the wound). Intervention 2: Intervention group: After washing the wo

Sponsors

Mashhad University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 50 Years

Inclusion criteria

Inclusion criteria: Degenerative Deep Partial-Thickness (Deep Second-Degree) burns between 5% and 20% From the time the burns up to the time of entry into the study is not more than 6 hours There are no underlying diseases and immune systems like diabetes, cancer, AIDS, hypertension, cardiovascular disease and peripheral neuropathy (neuropathy). The patient has no skin allergies Be alert and able to answer questions

Exclusion criteria

Exclusion criteria: Age is more than 50 years old Age is less than 15 years old

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: Before and after dressing - Day 1 and 3, 7 and 10. Method of measurement: Visual Analogue Scale.;Infection. Timepoint: Daily after opening the dressing. Method of measurement: Clinical checklist for localized infection of burn wound.;Clonization. Timepoint: Days 1, 3, 7 and 10. Method of measurement: Send the sterile swab specimen to the microbiological laboratory.

Secondary

MeasureTime frame
Prepare the wound for graft. Timepoint: Daily after opening the dressing. Method of measurement: The creation of granulation tissue in the wound area.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactHamid Chamanzari

Mashhad University of Medical Sciences

chamanzarih@mums.ac.ir+98 51 3859 1511

Outcome results

None listed

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