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.
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
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 group | Role | What they receive |
|---|---|---|
| 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. Receives: 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. Receives: Other: data collection |
What is being measured
The primary outcome is the main question the study is designed to answer.
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)
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
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
body distribution
Evaluate which body areas are most affected by the disease, and establish whether involvement in certain areas predicts treatment failure.
Measured: Baseline
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
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.
- First posted26 Dec 2025
- Study start7 Jan 2025
- Primary completion31 Dec 2025
- Study completion31 Dec 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for ScabiesStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Societa Italiana di Dermatologia Medica, Chirurgica, Estetica e di Malattie Sessualmente Trasmesse
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
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
Study at a glance
From the registry record, last updated by the sponsor on 27 Mar 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Studio Nazionale Sull'Epidemiologia ed Efficacia Delle Terapie Nel Trattamento Della Scabbia
- ClinicalTrials.gov ID
- NCT07305961
- Acronym / sponsor ID
- SCAB-net / SID06
- Conditions
- Scabies
- Study type
- Observational
- Recruitment status
- Completed
- Enrolment
- 1,332 participants (actual)
- Lead sponsor
- Societa Italiana di Dermatologia Medica, Chirurgica, Estetica e di Malattie Sessualmente TrasmesseUniversity, hospital or other
- Study start
- 7 Jan 2025 (actual)
- Primary completion
- 31 Dec 2025 (actual)
- Study completion
- 31 Dec 2025 (actual)
- First posted
- 26 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Multicentre retrospective, prospective, non-profit, national observational study
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.
Study design
- Observational model
- Cohort
- Time perspective
- Other
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| prospective cohort | – | Other: data collectionPatients 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. |
| retrospective cohort | – | Other: data collectionOnly the number of registered scabies cases and the presence or absence of treatment failures will be considered; no clinical patient data will be extrapolated. |
Who may qualify
- Ages
- 6 months to 99 years
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- 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.
Key inclusion criteria (3 listed)
- 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.
Key exclusion criteria (1 listed)
- There are no exclusion criteria.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| data collectionBiographical 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. | Other | prospective cohort |
| data collectionOnly 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. | Other | retrospective cohort |
Primary outcome
Healing Rate
Time frame: From the date of enrolment until the date of healing, assessed up to 52 weeks.
The cure rate is represented by the number of patients who were cured after the first treatment.
5 secondary outcomes
Frequency of scabies diagnosis
Time frame: From the date of enrolment to the previous three years
Epidemiological analyses
Time frame: at the end of the study
body distribution
Time frame: Baseline
presence/absence of clinical parameters
Time frame: Baseline
presence/absence of language barriers
Time frame: Baseline
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 27 Mar 2026.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
23 sites in 1 country: see every site and its status.
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.