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Effect of topical cream ,containing Tragacanth on the Eczema and it’s comparison with Mometasone 0.1%

Evaluating the efficacy of topical cream based on Iranian traditional medicine containing Tragacanth, White wax and Bitter almond oil on the symptoms management of Eczema (clinical study) and it’s comparison with Mometasone 0.1%

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20190914044767N1
Enrollment
42
Registered
2019-12-19
Start date
2019-12-21
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Mild to moderate hand eczema. Atopic dermatitis

Interventions

Intervention 1: Control group: The group receiving the cream is Momtazone 0.1% manufactured by Kish Medifarm Company in Iran. The cream is applied for 3 weeks every night and then for 2 weeks every ot

Sponsors

Traditional Medicine & Materia Medica Research center Shahid Beheshti university of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Men and women 18 years or older One or more eczema lesions in the palm or back area Mild to moderate plaques Patients who have not received topical, oral, or injectable medication for the treatment of eczema in the last week (emulsion use is permitted). Lack of infection or malignancy at the treatment site (no problem with closed wounds). Patient's consent to participate in the study

Exclusion criteria

Exclusion criteria: Under 18 years Pregnancy and lactation Eczema generalize Patients with other skin lesions Taking other topical medicines while participating in the research Patients taking immunosuppressive systemic drugs or biological drugs. Infection or skin malignancy at the treatment site

Design outcomes

Primary

MeasureTime frame
Atopic dermatitis disease intensity. Timepoint: At the beginning of the study and about 20 days after starting the topical cream (after treatment). Method of measurement: SCORAD Index form.;Duration of recovery. Timepoint: About 20 days after starting the topical cream (after treatment). Method of measurement: Patient Tracking and Evaluation with SCORAD and DLQI.

Secondary

MeasureTime frame
Quality of dermatology patient's life. Timepoint: At the beginning of the study and about 20 days after starting the topical cream (after treatment). Method of measurement: DLQI questionnaire.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactZahra Ghadimi

Islamic Azad University

Zahraghadimi1393@gmail.com+98 21 2264 0051

Outcome results

None listed

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