The effect of herbal ointment on second degree burn wound

Comparison of the effect of herbal ointment with silver sulfadiazine ointment on second degree burn wounds

Status

Recruiting

Phases

Phase 3

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190621043961N1

Enrollment

Registered

2019-10-03

Start date

2019-01-21

Completion date

Unknown

Last updated

2019-11-05

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

Conditions

second degree burn wound. Burn of second degree, body region unspecified

Interventions

Intervention 1: Intervention group: wound dressing with a thin layer of herbal ointment daily until the end of one month after the start of intervention. Intervention 2: Control group: wound dressing

Eligibility

Sex/Gender

All

Age

18 Years to No maximum

Inclusion criteria

Inclusion criteria: second degree burn wound age over 18 years less than 48 hours from the onset of burn injury Burn percentage less than 15% Informed consent to participation in research

Exclusion criteria

Exclusion criteria: Pregnant women Patients with severe systemic diseases such as epilepsy, diabetes, immune deficiency History of psychotic disorder such as paranoid; history of admission to psychiatry department Patients with a history of skin allergies to the components of the product Electrical and chemical burns Unwillingness to continue the intervention Allergy to Silver Sulfadiazine or Ointment Co-administration of antibiotics (oral and topical)

Design outcomes

Primary

Measure	Time frame
Recovery of burn wound. Timepoint: At first and the fourth day, then at the end of the first, second, third and fourth weeks. Method of measurement: photography and slide-calliper.	—

Secondary

Measure	Time frame
General wound appearance. Timepoint: days 1, 4, 7 and at the end of second, third and fourth weeks. Method of measurement: observation.;Pain. Timepoint: daily. Method of measurement: VAS scale.;Itching. Timepoint: daily. Method of measurement: Visual analog scale.;Inflamation. Timepoint: daily. Method of measurement: observastion.;Percentage of wound contraction. Timepoint: days 1, 4, 7 and at the end of second, third and fourth weeks. Method of measurement: photography and calliper.;Infection. Timepoint: daily. Method of measurement: observation.;Redness. Timepoint: daily. Method of measurement: observation.	—

Measure

Time frame

General wound appearance. Timepoint: days 1, 4, 7 and at the end of second, third and fourth weeks. Method of measurement: observation.;Pain. Timepoint: daily. Method of measurement: VAS scale.;Itching. Timepoint: daily. Method of measurement: Visual analog scale.;Inflamation. Timepoint: daily. Method of measurement: observastion.;Percentage of wound contraction. Timepoint: days 1, 4, 7 and at the end of second, third and fourth weeks. Method of measurement: photography and calliper.;Infection. Timepoint: daily. Method of measurement: observation.;Redness. Timepoint: daily. Method of measurement: observation.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMehdi Alizadeh

Shahid Beheshti University of Medical Sciences

m_alizadeh@sbmu.ac.ir+98 21 8877 3521

Outcome results

None listed

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