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The effect of herbal root of the Arnebia euchroma ointment on second degree burn wound healing

Comparison of herbal root of the Arnebia euchroma ointment and silver sulfadiazine on second degree burn wound

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT201412154492N2
Enrollment
30
Registered
2015-02-23
Start date
2014-12-16
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

Condition 1: Burn and corrosion of head and neck. Condition 2: Burn and corrosion of trunk. Condition 3: Burn and corrosion of shoulder and upper limb. Condition 4: Burn and corrosion of wrist and hand. Condition 5: Burn and corrosion of hip and lower limb. Condition 6: Burn and corrosion of ankle and foot. Burn of second degree of head and neck Burn of second degree of trunk Burn of second degree of shoulder and upper limb Burn of second degree of wrist and hand Burn of second degree of hi

Interventions

Intervention 1: A burned patient will be treated daily with tiny layer of the Arnebia euchroma ointment 10% on one part of the wound area. This process will be continued to complete of wound healin
Treatment - Drugs
A burned patient will be treated daily with tiny layer of the Arnebia euchroma ointment 10% on one part of the wound area. This process will be continued to complete of wound healing.
A burned patient will be treated daily with tiny layer of Silver sulfadiazine 1% on the second part of the wound are. This process will be continued to complete of wound healing.

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
16 Years to 65 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: bilateral second degree burn wound; aged 16 to 65 years. Exclusion criteria: pregnant women; existing of systemic disease such as diabetic patients; Cardiovascular disease; hypertension; Renal failure; Skin sensitivity; no willingness to participate.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Wound size. Timepoint: First day of burn injury; The third day; The fifth day; The seventh day; The tenth day; The twelfth day; The fifteenth day; The twentieth day; Twenty- fifth day; The thirtieth day. Method of measurement: By photograph and ruler.

Secondary

MeasureTime frame
Infection. Timepoint: daily. Method of measurement: observation.;Pain. Timepoint: daily. Method of measurement: VAS scale.;Itching. Timepoint: daily. Method of measurement: Visual analog scale.;Secretion. Timepoint: during daily dressing. Method of measurement: Observation.;Inflammation. Timepoint: daily. Method of measurement: Observation.;Redness. Timepoint: daily. Method of measurement: observation.;Burning. Timepoint: daily during dressing. Method of measurement: Visual analoge Scale.;Percentage wound contraction. Timepoint: each two days. Method of measurement: photography and ruler.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Sayed Jalal Hosseinimehr

Mazandaran University of Medical Sciences

sjhosseinim@yahoo.com or sjhosseinim@mazums.ac.ir+98 11 3354 4308

Outcome results

None listed

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