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Effect of Agicoat(silver nanocrystal dressing) in burn wound

Determination of effect of silver nanocrystal dressing (Agicoat) in second degree burn patients of Motahhari hospital and camparision it with Acticoat and silver sulfadiazine

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT201206237913N2
Enrollment
82
Registered
2012-10-08
Start date
2012-10-22
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. Corrosions of multiple regions, no more than second-degree corrosions mentioned

Interventions

Intervention 1: Dressing with silver sulfadiazine daily (closed dressing): the ointment will apply daily and with sterile gauze will close. Intervention 2: Acticoat dressing apply after wetting it by
Treatment - Drugs
Dressing with silver sulfadiazine daily (closed dressing): the ointment will apply daily and with sterile gauze will close
Acticoat dressing apply after wetting it by distilled water and fixing it to bed by tape and melonin and moistuering it by distilled water every 6 hours.The dressing will change every 4 days till woun
Agicoat dressing will undertake after wetting it by distilled water and applying itver wound. The first dressing change will take place after 72 hours or when there is discharge from wound.If there is

Sponsors

Emad pharmacy co.
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criterias : 1- 2nd degree burn between 15- 40% Exclusion criterias : 1- Unresidency of patients in Tehran 2- Underlying medical diseases 3- Sensitivity to Ag 4- Young and old ages: under 5 and over 65 years old

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Scar. Timepoint: 1 mo and 3mo and 6mo after discharge. Method of measurement: Vancover scar scale scor.;Wound epithelialization. Timepoint: 1wk after intervention and every 3days till 6wk. Method of measurement: Day.;Admission duration. Timepoint: Discharge date. Method of measurement: Discharge date minus admission date.;Infection. Timepoint: From time of admission till 1 mo after discharge. Method of measurement: Culture- biopsy.;Pain severity. Timepoint: Every 3 days till discharge date. Method of measurement: Visual analogue scale.;Expenditure. Timepoint: At discharge date. Method of measurement: Rial.

Secondary

MeasureTime frame
Ethiology. Timepoint: Admission time. Method of measurement: Scald, Fire.;Burn percentage. Timepoint: Admission time. Method of measurement: Tatal body surface burned.;Age. Timepoint: Admission time. Method of measurement: Year of entrance to study minus birth day.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadrza Akhoondinasab

Tehran University of Medical Sciences

burncenter_89@yahoo.com+98 21 8877 0031

Outcome results

None listed

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