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ScabiesSCAB-netNCT07305961

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

An observational study of Scabies, run by Societa Italiana di Dermatologia Medica, Chirurgica, Estetica e di Malattie Sessualmente Trasmesse at 23 sites in Italy.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

Multicentre retrospective, prospective, non-profit, national observational study Read more about this study

Who is it for?
Ages 6 months to 99 years
Conditions the study is for
Scabies
What is being tested?
data collection
How many people
1,332 participants
Where
23 sitesItaly
Study dates
7 Jan 2025to 31 Dec 2025
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 months to 99 years
  • All sexes
  • No healthy volunteers
  • Child, Adult, Older adult

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.

Who may be able to join

  • 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 informed consent.

Who cannot join

  • There are no exclusion criteria.

Trial locations and contacts

23 sites in 1 country.

23 sites in 1 country

Italy23 sites
  • Ospedale Cardinal Massaia

    Asti, AT, 14100

  • ASST Papa Giovanni XXIII

    Bergamo, BG, 24127

  • IRCCS AOU di Bologna

    Bologna, BO, 40138

  • AOU San Giovanni di Dio

    Cagliari, Italy, CA, 09123

  • USL Toscana Centro

    Florence, FI, 50100

  • Azienda Ospedaliera Universitaria Meyer IRCCS

    Florence, FI, 50139

  • Ospedali Riuniti di Foggia

    Foggia, FG, 71122

  • Ospedale Policlinico San Martino

    Genova, GE, 16132

  • ASST LECCO Alessandro Manzoni

    Lecco, LC, 23900

  • Ospedale Versilia

    Lido di Camaiore, LU, 55041

  • ASL Toscana Nord Ovest

    Lucca, LU, 55100

  • AOU Policlinico Gaetano Martino

    Messina, Maine, 98124

  • Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico

    Milan, Michigan, 20122

  • Università VANVITELLI

    Naples, 80138

  • AOU Maggiore della Carità

    Novara, 28100

  • Fondazione Policlinico San Matteo IRCCS

    Pavia, PV, 27100

  • AUSL Della Romagna

    Ravenna, RA, 48121

  • Fondazione Policlinico Tor Vergata

    Roma, RM, 00133

  • Istituto San Gallicano

    Roma, RM, 00144

  • Regina Margherita Children's Hospital, Città della Salute e della Scienza di Torino

    Torino, TO, 10126

  • APSS - Ospedale Santa Chiara

    Trento, Italy/Trento, 38123

  • AOU S.Maria della Misericordia

    Udine, UD, 33100

  • Ospedale Civico Maggiore Borgo Trento

    Verona, VR, 37126

Other trials in Italy

About this study

Official title: Studio Nazionale Sull'Epidemiologia ed Efficacia Delle Terapie Nel Trattamento Della Scabbia

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.

Conditions
Scabies
Being tested
data collection
Medical subject headings
Scabies

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • data collectionOther

    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.

  • data collectionOther

    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.

Study groups in NCT07305961
Study groupRoleWhat they receive
prospective cohortPatients 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.
Receives: Other: data collection
retrospective cohortOnly the number of registered scabies cases and the presence or absence of treatment failures will be considered; no clinical patient data will be extrapolated.
Receives: Other: data collection

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Healing Rate

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

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

Secondary outcomes (5)
  1. Frequency of scabies diagnosis

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

    Measured: 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.

    Measured: 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.

    Measured: 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.

    Measured: 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.

    Measured: Baseline

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Dec 2025
  2. Study start7 Jan 2025
  3. Primary completion31 Dec 2025
  4. Study completion31 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Other
Enrolment
1,332 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07305961
Sponsor's protocol ID
SID06
Other IDs
RSO ID - 477
Acronym
SCAB-net
Status last verified
Mar 2026
First submitted
13 Jun 2025
Last updated
27 Mar 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No

Questions about this trial

What is this clinical trial studying?

An observational study of Scabies, run by Societa Italiana di Dermatologia Medica, Chirurgica, Estetica e di Malattie Sessualmente Trasmesse at 23 sites in Italy.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 27 Mar 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 23 sites in Italy. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Healing Rate (time frame: From the date of enrolment until the date of healing, assessed up to 52 weeks.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 27 Mar 2026.

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