The effect of the sertaconazole cream with ointment Hydrocortisone in atopic dermatitis

Comparison of the therapeutic effect of sertaconazole cream with Hydrocortisone ointment on atopic dermatitis in children under five years

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

IRCT

Registry ID

IRCT20190624043996N1

Enrollment

Registered

2020-01-13

Start date

2019-06-01

Completion date

Unknown

Last updated

2020-02-24

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: Intervention 1: 2% sertaconazole cream, topical antifungal at a dose of the size of the skin involved two times a day for two weeks, topical application on the skin by hand, Farer Inte

Eligibility

Sex/Gender

All

Age

No minimum to 5 Years

Inclusion criteria

Inclusion criteria: Children under five years with atopic medium or mild dermatitis

Exclusion criteria

Exclusion criteria: The lack of parental consent Atopic dermatitis with sever involvement of the skin

Design outcomes

Primary

Measure	Time frame
Medication type. Timepoint: The primary visit is at the beginning of the study before initiating the therapy. The second, third, and fourth visits were made two weeks, one month, and six months after the start of the treatment, respectively. Method of measurement: Measuring variables involved three visits and patient examination by clinical research at a specified time, as well as completing a questionnaire and table relating to the symptoms. The questionnaire and table of symptoms were derived from previous valid articles and scientific references.	—

Measure

Time frame

Medication type. Timepoint: The primary visit is at the beginning of the study before initiating the therapy. The second, third, and fourth visits were made two weeks, one month, and six months after the start of the treatment, respectively. Method of measurement: Measuring variables involved three visits and patient examination by clinical research at a specified time, as well as completing a questionnaire and table relating to the symptoms. The questionnaire and table of symptoms were derived from previous valid articles and scientific references.

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Countries

Iran (Islamic Republic of)

Contacts

Public ContactFazel Ali

Yasouj University of Medical Sciences

Ali.fazel@yums.ac.ir+98 74 3334 5868

Outcome results

None listed

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