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CompletedNCT07305961SCAB-netUpdated Mar 27, 2026

National Study on the Epidemiology and Effectiveness of Therapies in the Treatment of Scabies

An observational study in Scabies, sponsored by Societa Italiana di Dermatologia Medica, Chirurgica, Estetica e di Malattie Sessualmente Trasmesse. Completed at 23 sites in Italy. Open to participants aged 6 Months to 99 Years. Per ClinicalTrials.gov, last updated 2026-03-27.

Sponsored by Societa Italiana di Dermatologia Medica, Chirurgica, Estetica e di Malattie Sessualmente Trasmesse · Observational

Study type
Observational
Model
Cohort
Time perspective
Other
Enrollment
1,332
Ages
6 Months to 99 Years
Sex
All
01

Study summary

Multicentre retrospective, prospective, non-profit, national observational study

Read the detailed description

Scabies is an infectious skin condition caused by the mite Sarcoptes scabiei var. hominis. This mite can only parasitise and reproduce in the outermost layer of human skin (the stratum corneum). The disease is typically transmitted through human-to-human contact, though it can also be transmitted through fomites. It affects between 200 and 300 million people worldwide each year, with considerable variation in prevalence ranging from 0.2% to 71.4% in different regions. Over the past 10-20 years, the frequency of epidemics appears to be increasing, not only in countries where scabies is prevalent, but also in states that have historically experienced low rates of infection.The increase in cases across Europe, coupled with the rapid epidemic spread of the disease and the emergence of resistance to topical treatments, underscores the imperative for a comprehensive and systematic study involving multiple centres.

The primary guidelines for managing scabies involve performing environmental hygiene measures, such as washing and changing clothing daily and cleaning all surfaces that come into contact with the skin.

In terms of treatment, the European Society of Dermatology and Venereology guidelines recommend topical permethrin or benzyl benzoate and oral ivermectin as first-line treatments.

Apply topical permethrin 5% cream in the evening to cool, dry skin all over your body, including the folds, navel, limbs, genitals, the area behind your ears and under your nails. If there are any suspicious lesions, the scalp and face should also be treated, avoiding the areas around the eyes and lips. Leave the cream in place for 8-12 hours and apply a second dose after 7-14 days.

Oral ivermectin should be taken as a single dose at a dosage of 200 μg/kg, repeated in the same manner after seven days. Although European guidelines recommend taking it on a full stomach, the manufacturer and other guidelines recommend taking it on an empty stomach.

Benzyl benzoate lotion at a concentration of 10-25% is applied for two evenings and left in place for 8-12 hours. A third application should be made after seven days.

The treatment should be carried out not only by the patient, but also by their close contacts - usually members of their household - and should be extended to anyone who has had prolonged and continuous contact with individuals who are ill.

Topical permethrin cream at 5% is the first-line treatment for scabies in Italy. However, there has recently been an increase in reports of treatment failure. This phenomenon has also become increasingly prevalent in many other European countries. Therapy failure is likely to be due to a combination of factors, including drug resistance. Incorrect use of the treatment in terms of the amount of active ingredient, the method of application and/or the timing could be the cause of treatment failure.

The increase in cases in Europe, the rapid spread of the disease and the growing phenomenon of treatment resistance highlight the need for a large, systematic study involving several centres. Therefore, we propose a national multicentre retrospective and prospective observational study that aims to evaluate epidemiological data (prevalence, incidence, affected ethnicities and population groups), the most frequently used treatments, and treatment failures.

This study aims to evaluate the success rate of first-line therapies according to European guidelines in patients diagnosed with scabies and their close contacts (family members/caregivers). This will be achieved by observing patients with scabies who attend outpatient clinics for diagnosis, treatment and/or follow-up.

02

Conditions studied

  • Scabies

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03

In context

Scabies

51 studies on the registry are indexed under Scabies; 10 are open to participants now.

This study's enrollment of 1,332 is above the median of 775 across 10 observational studies indexed under Scabies.

Browse Scabies studies →

Lead sponsor

Societa Italiana di Dermatologia Medica, Chirurgica, Estetica e di Malattie Sessualmente Trasmesse is the lead sponsor of 6 studies on the registry; 4 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
6 Months to 99 Years
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

All patients with scabies and their close contacts (household/partners) afferent to the outpatient clinics of participating Italian centers during the duration of the study will be included in the study.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Patients of any age with clinical and/or dermoscopic and/or microscopic diagnosis of scabies.
  • Close contacts (household/relatives) of patients diagnosed with scabies.
  • Obtaining .

Exclusion criteria

Exclusion Criteria:

  • There are no exclusion criteria.
Terms in these criteria, in plain language(1)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

Informed consent

Before you join, the study team explains what taking part involves — its purpose, what happens, the risks and possible benefits — and answers your questions, so you can decide freely. Consent is usually recorded on a form (the informed consent form, ICF) signed by you or, where the law allows, by someone legally authorised to decide for you.

You can keep asking questions during the study, you are told of new information that matters, and you can choose to leave at any time.

05

Study design

Observational model
Cohort
Time perspective
Other
Enrollment
1,332 participants (actual)
Patient registry
No

Groups and cohorts

  • prospective cohort

    Patients diagnosed with scabies who attend outpatient clinics and their close contacts (household members and partners) at the various participating centres from the date of study approval until 31/12/2025 will be included, along with additional parameters regarding treatment, failures and epidemiological and clinical assessments.

    Other: data collection

  • retrospective cohort

    Only the number of registered scabies cases and the presence or absence of treatment failures will be considered; no clinical patient data will be extrapolated.

    Other: data collection

Interventions

  • Otherdata collection

    Biographical data: age; immunodeficiency; bedridden condition. Household data: number of people in the household, original state of the household, presence of paediatric cases weighing more or less than 15 kg, presence of a language barrier. Diagnostic criteria: clinical, dermatoscopic and/or microscopic. Clinical data: affected areas, non-specific therapies previously carried out. Days of isolation of the index case (if applicable). Treatment data: the first specific anti-mite therapy carried out, including the mode of administration; the number of days since the onset of the illness; the number of people treated per index case; the drug with which recovery was achieved (if known); and the time taken for recovery. Data for investigating treatment failures: answers to questions concerning treatment carried out with close contacts and cohabitants, correct information about environmental remediation implementation, number of therapy cycles carried out and follow-up timeframe.

  • Otherdata collection

    Only the number of registered scabies cases and whether or not treatment has failed will be taken into account. No clinical data from the patients will be extrapolated.

06

What researchers measure

Primary outcomes

  1. Healing Rate

    The cure rate is represented by the number of patients who were cured after the first treatment.

    Time frame: From the date of enrolment until the date of healing, assessed up to 52 weeks.

Secondary outcomes

  1. Frequency of scabies diagnosis

    Assess the trend in the absolute frequency of scabies diagnoses over the past three years.

    Time frame: From the date of enrolment to the previous three years

  2. Epidemiological analyses

    Conduct descriptive epidemiological analyses by categorising the observed cases according to age group, ethnicity, and time distribution over the study period.

    Time frame: at the end of the study

  3. body distribution

    Evaluate which body areas are most affected by the disease, and establish whether involvement in certain areas predicts treatment failure.

    Time frame: Baseline

  4. presence/absence of clinical parameters

    Evaluate the clinical parameters of the index case, such as immunodepression and allurement. Consider whether any previous non-specific therapies may have increased the likelihood of treatment failure.

    Time frame: Baseline

  5. presence/absence of language barriers

    Evaluate whether a language barrier exists between healthcare workers and patients, as incorrect intake of therapy in terms of dosage and timing, as well as a lack of or incorrect environmental hygiene measures, may be correlated with treatment failure or re-infestation.

    Time frame: Baseline

07

Study locations

23 sites
  • Ospedale Cardinal Massaia
    Asti, AT 14100, Italy
  • ASST Papa Giovanni XXIII
    Bergamo, BG 24127, Italy
  • IRCCS AOU di Bologna
    Bologna, BO 40138, Italy
  • Ospedali Riuniti di Foggia
    Foggia, FG 71122, Italy
  • USL Toscana Centro
    Florence, FI 50100, Italy
  • Azienda Ospedaliera Universitaria Meyer IRCCS
    Florence, FI 50139, Italy
  • Ospedale Policlinico San Martino
    Genova, GE 16132, Italy
  • AOU San Giovanni di Dio
    Cagliari, Italy, CA 09123, Italy
  • APSS - Ospedale Santa Chiara
    Trento, Italy/Trento 38123, Italy
  • ASST LECCO Alessandro Manzoni
    Lecco, LC 23900, Italy
  • Ospedale Versilia
    Lido di Camaiore, LU 55041, Italy
  • ASL Toscana Nord Ovest
    Lucca, LU 55100, Italy
  • AOU Policlinico Gaetano Martino
    Messina, Maine 98124, Italy
  • Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico
    Milan, Michigan 20122, Italy
  • Fondazione Policlinico San Matteo IRCCS
    Pavia, PV 27100, Italy
  • AUSL Della Romagna
    Ravenna, RA 48121, Italy
  • Fondazione Policlinico Tor Vergata
    Roma, RM 00133, Italy
  • Istituto San Gallicano
    Roma, RM 00144, Italy
  • Regina Margherita Children's Hospital, Città della Salute e della Scienza di Torino
    Torino, TO 10126, Italy
  • AOU S.Maria della Misericordia
    Udine, UD 33100, Italy
  • Ospedale Civico Maggiore Borgo Trento
    Verona, VR 37126, Italy
  • Università VANVITELLI
    Naples, 80138, Italy
  • AOU Maggiore della Carità
    Novara, 28100, Italy
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 27, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07305961
Lead sponsor
Societa Italiana di Dermatologia Medica, Chirurgica, Estetica e di Malattie Sessualmente Trasmesse
Responsible party
Sponsor
First posted
Dec 26, 2025
Start date
Jan 7, 2025
Primary completion
Dec 31, 2025
Completion
Dec 31, 2025
Last update
Mar 27, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2026. You cannot join it, but the record below documents what was studied.

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