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The effect of Althaea officinalis ,local product on burns wounds

The effect of Althaea officinalis L. local product on healing parameters of superficial burn wounds

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20251012067604N1
Enrollment
80
Registered
2025-11-08
Start date
2025-11-06
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Second-degree burns. Burn and corrosion of shoulder and upper limb, except wrist and hand

Interventions

Intervention 1: Intervention group: A burned limb will be dressed using 1% sulfadiazine ointment, according to hospital routine, and its counterpart will be dressed using Althaea officinalis ointment.

Sponsors

Tabriz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Patients who have burns of 20% or less in area and with a depth of 2nd degree, and the cause of the patient's burn is other than chemical or electrical materials, and the patients do not have inhalation injuries. The burn site on the limbs should be symmetrical and of the same depth. No more than 3 hours have passed since the burn occurred and the patient is able to answer questions.

Exclusion criteria

Exclusion criteria: Lactating and pregnant women Patients with medical diseases such as diabetes mellitus, allergic skin diseases, malignancy, AIDS, hypertension, etc. History of use of cytotoxic drugs or history of allergy to herbal products If the wound is contaminated with contaminants Use of materials on the patient's wound (other than drinking water) before entering the study If patients are referred to Sina Medical Center after being admitted and receiving care at another medical center, they will not be included in the study.

Design outcomes

Primary

MeasureTime frame
Wound healing. Timepoint: One, seven, fourteen and twenty-eight days after the first dressing. Method of measurement: Bats Jenson questionnaire.;Wound-related pain. Timepoint: Daily, before dressing, half an hour after dressing, and at 8 p.m. Method of measurement: Visual Analogue Scale.;Itching related to the wound. Timepoint: One, seven, fourteen and twenty-eight days after the first dressing. Method of measurement: Visual Analog Scale.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMasume Lotfi kahagh

Tabriz University of Medical Sciences

lotfi-kahagh@tbzmed.ac.ir+98 41 3337 9527

Outcome results

None listed

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