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Efficacy of Tacrolimus ointment in the treatment of tinea versicolor

Comparison of the efficacy of Tacrolimus ointment and Clotrimazole cream in the treatment of tinea versocolor

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
IRCT
Registry ID
IRCT2014021216557N1
Enrollment
50
Registered
2016-06-30
Start date
2014-04-21
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

Pityriasis versicolor. Pityriasis versicolor

Interventions

Intervention 1: Intervention: Application of Tacrolimus 0.03% ointment two times a day for 21 days. Intervention 2: Control: Application of Clotrimazole 1% cream two times a day for 21 days.
Treatment - Drugs
Intervention: Application of Tacrolimus 0.03% ointment two times a day for 21 days
Control: Application of Clotrimazole 1% cream two times a day for 21 days

Sponsors

Research Council of Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
10 Years to 100 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Clinical diagnosis of tinea versicolor; Confirmation of diagnosis by Wood's lamp examination (Yellow fluorescence) and Direct smear; Patients of 10 year old and over; Less than 15% of body surface area involvement Exclusion criteria: Pregnancy or Lactation; History of hypersensitivity to main or preservative ingredients of topical tacrolimus or clotrimazole; Serious skin or systemic diseases; History of consumption of topical or systemic antifungal medications in the recent 1 month before enrolling in study

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Wood's lamp fluorescence. Timepoint: 0, 3rd, and 5th week. Method of measurement: Wood's lamp radiation.;Scale and hyperpigmentation grade. Timepoint: 0, 3rd, and 5th week. Method of measurement: Physician global assessment.;Malassezia species positivity. Timepoint: o, 3rd and 5th weeks. Method of measurement: Direct KOH 10% smear.

Secondary

MeasureTime frame
Pruritus. Timepoint: 0, 3rd, and 5th week. Method of measurement: Visual assessment scale.;Hypopigmentation. Timepoint: 0, 3rd, and 5th week. Method of measurement: Physician global assessment.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMaryam Sadat Sadat

Shiraz University of Medical Sciences

m_sadat63@yahoo.com+98 71 3212 5239

Outcome results

None listed

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