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Efficacy of topical azathioprine-betamethasone cream with betamethasone cream in cutaneous eczema

Comparison of the efficacy of combined therapy with topical azathioprine and betamethasone emollient cream versus monotherapy with topical betamethasone emollient cream in 2-18 year-old patients with moderate to severe atopic dermatitis.

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014092519292N1
Enrollment
70
Registered
2014-11-14
Start date
2013-11-22
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

Atopic dermatitis. Atopic dermatitis

Interventions

Intervention 1: Patients in intervention group should use the azathioprine-betamethasone emolient cream twice daily for 8 weeks on cutaneous lesions of the whole body except for face. Intervention 2:
Treatment - Drugs
Patients in intervention group should use the azathioprine-betamethasone emolient cream twice daily for 8 weeks on cutaneous lesions of the whole body except for face.
Patients in control group should use betamethasone emolient cream twice daily for 8 weeks on all cutaneous lesions of the body except for face.

Sponsors

Vice Chancellor for research of Isfahan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 18 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: children older than 2 years; patients with no enough response to conventional topical therapies in recent past 6 months; patients who do not receive any systemic drug which interacts with azathioprine in recent past 1 month; patients whose lesions are not limited to the face; patients with out any liver and bone marrow dysfunction. Exclusion criteria: any labratory abnormality; patients who do not desired to stay in the study.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Clinical severity of cutaneous lesions. Timepoint: At baseline, at the end of the treatment course(8th week), one month after the cessation of the treatment. Method of measurement: SCORAD index.

Secondary

MeasureTime frame
Recurrence of cutaneous lesions. Timepoint: 1 month after the cessation of the treatment. Method of measurement: Physical exam and history taking.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Sadaf Farhadi

Skin disease and Leishmaniasis Research Center, Isfahan University of Medical Sciences

sadaffarhadi@resident.mui.ac.ir www.mui.ac.ir+98 31 3785 0842

Outcome results

None listed

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