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Assessing the effectiveness of Sambucus Ebulus ointment in treatment of Leishmaniasis

Assessing the effectiveness of Sambucus Ebulus ointment in treatment of Leishmaniasis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20171028037044N4
Enrollment
90
Registered
2018-01-26
Start date
2017-11-30
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

cutaneous leishmaniasis. Cutaneous leishmaniasis

Interventions

Intervention 1: Intervention group: Sambucus Ebulus 5 % ointment two times a day a layer until the full lesion epithelialization or up to 4 weeks after last intervention. Intervention 2: Control group
Treatment - Drugs
Placebo
Intervention group: Sambucus Ebulus 5 % ointment two times a day a layer until the full lesion epithelialization or up to 4 weeks after last intervention
Control group: Placebo ointment two times a day a layer until the full lesion epithelialization or up to 4 weeks after last intervention

Sponsors

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

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with lesions which lasts more than 14 days and definitely diagnosed cutaneous leishmaniasis by parasites seen in smears taken from skin lesions, and treating by the national standard treatment guidelines.

Exclusion criteria

Exclusion criteria: Pregnant women, patients with allergy to antimuan, patients taking more than three months have passed since the first appearance of skin lesions, patients in recent months any way be used to treat leishmaniasis, patients which their wound on the eyelids, ear, nose or are less than one centimeter is near the end of the lips and eyes.

Design outcomes

Primary

MeasureTime frame
Longest diameter of ulceration area. Timepoint: 0,7,14,21,28 day& if not cured 4 week after last intervention. Method of measurement: Ruler.;Longest diameter of Induration area. Timepoint: 0,7,14,21,28 day& if not cured 4 week after last intervention. Method of measurement: Ruler.;Healing rate. Timepoint: 0,7,14,21,28 day& if not cured 4 week after last intervention. Method of measurement: Observation & calculation.;Treatment resualt. Timepoint: At the end of treatmen, and if lesion not full epithelialized 4 weeks after last intervention. Method of measurement: Observation & determination.

Secondary

MeasureTime frame
Side effect. Timepoint: During treatment. Method of measurement: Observation & interview.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactOmid Mozafari

Golestan University of Medical Sciences

dr.mozafari@goums.ac.ir+98 17 3322 5124

Outcome results

None listed

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