The effect of Acticoat and usual dressing on Wound healing and burnt patients’ pain.

Comparison the effect of regular dressing and Acticoat on wound healing and pain in patients admitted to hospital for treatment of burns at Clinic Vali Asr (aj), Arak 2010-2012

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2012123111940N2

Enrollment

Registered

2013-09-07

Start date

2010-03-20

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Burn. Burns and corrosions of external body surface, specified by site

Interventions

Intervention 1: The experimental group was treated with Acticoat dressing l for two weeks. Intervention 2: The control group was treated with Sulfadiazine 1% for two weeks.

Treatment - Drugs

The experimental group was treated with Acticoat dressing l for two weeks

The control group was treated with Sulfadiazine 1% for two weeks.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Inclusion criteria were: all burn patients with the following conditions have been chosen as examples: 1)the subjects burned grade 2, grade 3, or a combination, of less than 15% body surface area burns were. 2) ulcer patients not treated with contaminated materials. Before entering the study, samples of any substance other than potable water were not used on wounds. 3) All subjects before entering the study were infected symptomatic of the body. 4) None of the participants in the research underlying immune deficiency diseases such as diabetes, cancer, AIDS, and high blood pressure. .... Did not. 6) willingness to participate in the study were injection molded, and able to answer questions. Exclusion criteria were: 1) Patients who were admitted to the burn unit. 2) After approval of the study, patients were withdrawn from treatment. 3) In case of any allergies or sensitivity to drug treatment. 4) In case of any signs of wound infection in spite of treatment.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Wound healing. Timepoint: days 1, 7 and 15. Method of measurement: The wound assessment tool Baets - Jensen.;Pain at dressing change. Timepoint: Days 1,7 and 15. Method of measurement: Using the Numeric Pain tool.	—

Secondary

Measure	Time frame
Pain. Timepoint: days 1, 7 and 15. Method of measurement: Using the Numeric Pain tool.	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzam malekhoseini

Arak University of Medical Sciences

malekhoseni.aram@gmail.com+86 12267892

Outcome results

None listed

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