" Study of the effectiveness of Bilva ointment on burn wound outcomes of patients admitted"

" Study of the effectiveness of Bilva ointment on burn wound outcomes of patients admitted "

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT20160424027561N11

Enrollment

Registered

2018-08-30

Start date

2017-03-20

Completion date

Unknown

Last updated

2018-09-11

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

Conditions

burn wound outcomes of patients admitted. Corrosion of second degree of shoulder and upper limb, except wrist and hand

Interventions

Intervention 1: In the intervention group, after washing the wound with water, the Bilva ointment made in Tabnak company is used and then it is bandaged. Intervention 2: Control group: In the control

Eligibility

Sex/Gender

All

Age

18 Years to 60 Years

Inclusion criteria

Inclusion criteria: Patients with 20% or less burns of second degree The location of the burn in the symetric extremities with the same depth Patients who do not have any underlying disease such as diabetes mellitus, allergic skin diseases, malignancy, AIDS, hypertension, and cytotoxic drugs. It is not more than 2 hours from the time of burning up to the time of entry into the research The patient's wound is not impregnated with contaminants The patient did not use any substance other than drinking water on the wound before the sample entered the study Before entering the study, the patient is not infected with different parts of the body The patient is able to answer questions.

Exclusion criteria

Exclusion criteria: The cause of the patient's burn is chemical or electrical. Patients who have inhaling injuries

Design outcomes

Primary

Measure	Time frame
Burn wound healing score. Timepoint: Day one, seventh, fourteenth, twenty eight, one month later, two months later, three months later. Method of measurement: Bates-Jensen wound assessment tool.;Pain. Timepoint: Day one, seventh, fourteenth, twenty eight, one month later, two months later, three months later. Method of measurement: Visual analogue scale (VAS).;Itching. Timepoint: Day one, seventh, fourteenth, twenty eight, one month later, two months later, three months later. Method of measurement: itching Visual analogue scale (VAS).;Infection. Timepoint: Day one, seventh, fourteenth, twenty eight, one month later, two months later, three months later. Method of measurement: questionnaire.;Hypertrophy of scar. Timepoint: one month later, two months later, three months later. Method of measurement: Vancouver questionnaire.	—

Measure

Time frame

Burn wound healing score. Timepoint: Day one, seventh, fourteenth, twenty eight, one month later, two months later, three months later. Method of measurement: Bates-Jensen wound assessment tool.;Pain. Timepoint: Day one, seventh, fourteenth, twenty eight, one month later, two months later, three months later. Method of measurement: Visual analogue scale (VAS).;Itching. Timepoint: Day one, seventh, fourteenth, twenty eight, one month later, two months later, three months later. Method of measurement: itching Visual analogue scale (VAS).;Infection. Timepoint: Day one, seventh, fourteenth, twenty eight, one month later, two months later, three months later. Method of measurement: questionnaire.;Hypertrophy of scar. Timepoint: one month later, two months later, three months later. Method of measurement: Vancouver questionnaire.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactMojghan Lotfi

Tabriz University of Medical Sciences

lotfim@tbzmed.ac.ir+98 41 3328 2085

Outcome results

None listed

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