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A Comparative Trial on Scabies Treatments: Topical Permethrin, Oral Ivermectin and Combination of Topical Permethrin and Oral Ivermectin

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2024-520348-40-00
Acronym
GIU_PER_IV_0024
Enrollment
156
Registered
2025-07-08
Start date
2025-10-02
Completion date
Unknown
Last updated
2025-07-08

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

Conditions

Clinical and light microscopy confirmed scabies

Brief summary

Percentage of subjects (Score 0; see below) with Complete cure rate (CCR) at Visit 1 (week 1)

Detailed description

Percentage of subjects (Score 0; see below) with Complete cure rate (CCR) at Visit 2 (week 2), Percentage of Subjects with score 0 or 1 at week 1, Percentage of subjects with CCR at week 2, Percentage of subjects with score 0 or 1 at week 2, Subjective evaluation of itching at week 1 and 2, Percentage of treatment failure at week 1 and week 2 (treatment failure is defined as: no improvement at all of itching intensity and skin lesions count and/or appearance of new lesions), Safety and Tolerability endpoints: (at week 1, week 2) - Evaluation and recording of spontaneous reported adverse events - Blood pressure monitoring - Heart rate

Interventions

DRUGSCABIACID 5% crema
DRUGIVERMECTINA GIULIANI 3 mg compresse

Sponsors

Giuliani S.p.A.
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Percentage of subjects (Score 0; see below) with Complete cure rate (CCR) at Visit 1 (week 1)

Secondary

MeasureTime frame
Percentage of subjects (Score 0; see below) with Complete cure rate (CCR) at Visit 2 (week 2), Percentage of Subjects with score 0 or 1 at week 1, Percentage of subjects with CCR at week 2, Percentage of subjects with score 0 or 1 at week 2, Subjective evaluation of itching at week 1 and 2, Percentage of treatment failure at week 1 and week 2 (treatment failure is defined as: no improvement at all of itching intensity and skin lesions count and/or appearance of new lesions), Safety and Tolerability endpoints: (at week 1, week 2) - Evaluation and recording of spontaneous reported adverse events - Blood pressure monitoring - Heart rate

Countries

Italy

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026