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Evaluation of the effectiveness of Brazambel extract in the treatment of cutaneous leishmaniasis

Evaluation of the effect of Perovskia abrotanoides extract in the treatment of cutaneous leishmaniasis: a randomized controlled clinical trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20150721023282N19
Enrollment
60
Registered
2021-08-06
Start date
2021-09-23
Completion date
Unknown
Last updated
2021-08-30

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: Topical ointment of Brazambel 10%, (made by Isfahan University of Medical Sciences), School of Pharmacy, once a day, with intralesional injection of Glucantime twic

Sponsors

Esfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
5 Years to No maximum

Inclusion criteria

Inclusion criteria: The incidence of sores in less than 5 numbers, confirmed by microscopic testing (observation of amastigots) or cultivation of discharge (presence of moving promastigots) Sideration (diameter) wound less than 5 centimeters

Exclusion criteria

Exclusion criteria: Mucosal involvement (mucous leishmanase) Systemic conflict (visceral leishmanase) Pregnancy Lactation Disease diffused Receiving an effective drug on Leishmania during recent 8 weeks (antifungal Azithromycin, allopurinol, aminoglycoside, amphotericine b, anti-compound) Skin disease associated with The existence of the lesion in ear, face or near the mucous district The secondary bacterial infection in the wound

Design outcomes

Primary

MeasureTime frame
Percent of decrease in lesion. Timepoint: Baseline, 7 and 14 Days after Initiation of Intervention. Method of measurement: Ruler.

Secondary

MeasureTime frame
The secondary outcome variable is the time required for complete recovery. Timepoint: Baseline, 7 and 14 Days after Initiation of Intervention. Method of measurement: Observation.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactRasool Soltani

Esfahan University of Medical Sciences

soltani@pharm.mui.ac.ir+98 31 3792 7067

Outcome results

None listed

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