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The effect of Sambucus ebulus in the treatment of Paederus Dermatitis

Evaluation of the effect of Sambucus ebulus 5% solution in the treatment of Paederus Dermatitis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
IRCT
Registry ID
IRCT201302132342N3
Enrollment
60
Registered
2013-03-09
Start date
2011-01-02
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

Paederus dermatitis. Irritant contact eczema NOS

Interventions

Intervention 1: Intervention group will receive S. ebulus fruit extract 5% solution and hydrocortisone ointment for locally 3 times a day. Intervention 2: Patients in control group will receive ethan
Treatment - Drugs
Intervention group will receive S. ebulus fruit extract 5% solution and hydrocortisone ointment for locally 3 times a day.
Patients in control group will receive ethanol 70° and hydrocortisone ointment for locally 3 times a day.

Sponsors

Mazandaran University of Medical Sciences, Vice-chancellor for research
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 60 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Age: 10-60 years; Diagnosis of Paederus dermatitis; Lasting at least 24 hours from the beginning wound signs. Exclusion criteria: Age out of mentioned range; Pregnancy; Diseases or drug using associated with impaired immune system or absence of natural skin repair

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Pain. Timepoint: At the beginning of study and then every 12 hours. Method of measurement: questionare.;Burning. Timepoint: At the beginning of study and then every 12 hours. Method of measurement: questionare.;Lesion size. Timepoint: At the beginning of study and then every 24 hours. Method of measurement: Centimeter square.

Secondary

MeasureTime frame
Treatment duration. Timepoint: The end of treatment. Method of measurement: Hour.;Incidence of infection. Timepoint: Each 24 hours. Method of measurement: Physician examination.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Mohahammadali Ebrahimzadeh

College of Pharmacy, Mazandaran University of Medical Sciences

zadeh20@yahoo.com+98 15 1354 3083

Outcome results

None listed

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