Sleep ApneaIPNOSNCT06872242
Italian PheNotypes Obstructive Sleep Apnea Study
An observational study of Sleep Apnea, run by Istituto Auxologico Italiano at 30 sites in Italy.
Trial summary
Obstructive Sleep Apnea (OSA) is the most common sleep-related breathing disorder, representing a major socioeconomic burden on healthcare systems worldwide. Studies performed in Europe in the last twenty years showed a very high prevalence and highlighted that the severity of untreated OSA worsens over time. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Sleep Apnea
- What is being tested?
- Polysomnography
- How many people
- 5,000 participants
- Where
- 30 sitesItaly
- Study dates
- 1 Jun 2024to 23 Oct 2025
- Phase
- Observational
- Are there results?
- Not yet: the study is under way
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 18 years and older
- All sexes
- Adult, Older adult
Study population: Adult patients referred to the Italian Sleep Centres because of suspected Obstructive Sleep Apnea
Who may be able to join
- Suspected Obstructive Sleep Apnea
- Age 18 years or older
Who cannot join
- Unstable psychiatric disease
- Limited life expectancy due to illness unrelated to sleep apnoea or other medical conditions which may interfere with the study protocol in the opinion of the investigator
Trial locations and contacts
30 sites in 1 country. Contact the study team or a site near you to ask about taking part.
30 sites in 1 country
Italy30 sites, 29 recruiting
- Recruiting
ASP Cosenza- PO Beato Angelico
Acri
Maria Ferraro, +390982 581264, maria.ferraro9@tin.it
- Not yet recruiting
AOU delle Marche
Ancona
Antonina Re, +390715964338, nirex1@yahoo.it
- Recruiting
AOU Policlinico di Bari
Bari
Elisiana Carpagnano, +3908055922907, elisiana.carpagnano@uniba.it
- Recruiting
ASST Papa Giovanni XXIII
Bergamo
Maria Cristina Servalli, +390352673296, mcservalli@hpg23.it
- Recruiting
Casa di cura San Francesco-Istituto Madre Rubatto
Bergamo
Anna Micheli, +393385327017, annamich1@virgilio.it
- Active, not recruiting
AUSL Bologna - Clinica odontoiatrica DIBINEM
Bologna
- Not yet recruiting
AUSL Bologna - Ospedale di Bellaria
Bologna
Federica Provini, +390514966990, federica.provini@unibo.it
- Recruiting
AOU Cagliari - Centro interdipartimentale dei disturbi del sonno
Cagliari
Stefania Redolfi, 070 675 3113, stefania.redolfi@unica.it
- Not yet recruiting
AOU Rodolico-S. Marco
Catania
Alberto Bianchi, +393357067060, alberto.bianchi@unict.it
- Recruiting
ASP Cosenza- P.O. di Rossano
Corigliano-Rossano
Miguel Angel Paludi, +393392033505, michele.paludi@aspcs.it
- Recruiting
Distretto Sanitario Cosenza- Savuto- Ambulatorio di Medicina del Sonno
Cosenza
Paola Elisa Scarpino, +3909848934852, p.scarpino@hotmail.it
- Recruiting
AOU Ospedali Riuniti di Foggia
Foggia
Pasquale Tondo, +393925078524, pasquale.tondo@unifg.it
- Recruiting
Opera Don Uva Universo Salute
Foggia
Maria Pia Foschino Barbaro, +393204394764, mariapia.foschino@unifg.it
- Not yet recruiting
IRCCS Ospedale Policlinico San Martino
Genova
Dario Arnaldi, +39105557130, dario.arnaldi@gmail.com
- Not yet recruiting
Ospedale Carlo Urbani
Iesi
Alessia Resedi, +390717130723, alessiaresedi@tiscali.it
- Recruiting
IRCCS Istituto Neurologico "Carlo Besta"
Milan
Giuseppe Didato, 02 23942576, giuseppe.didato@istituto-besta.it
- Recruiting
Istituto Auxologico Italiano
Milan
Carolina Lombardi, +3902619112750, c.lombardi@auxologico.it
- Recruiting
Ospedale San Paolo
Milan
Elena Zambrelli, +39 02 81844201, elena.zambrelli@asst-santipaolocarlo.it
- Not yet recruiting
AO dei Colli - PO Monaldi
Naples
Marialuisa Bocchino, +393334914670, marialuisa.bocchino@unina.it
- Recruiting
Ospedali Riuniti Villa Sofia Cervello
Palermo
Maria Rosaria Bonsignore, +3909123869203, mariarosaria.bonsignore@unipa.it
- Not yet recruiting
Azienda Ospedaliero-Universitaria di Parma
Parma
Liborio Parrino, +390521704107, liborio.parrino@unipr.it
- Recruiting
IRCCS Fondazione Mondino
Pavia
Michele Terzaghi, 0382 380335, michele.terzaghi@mondino.it
- Recruiting
Istituti Clinici Scientifici Maugeri
Pavia
Francesco Fanfulla, +390382592807, francesco.fanfulla@icsmaugeri.it
- Not yet recruiting
Casa di Cura "Villa Serena"
Pescara
Biancamaria Guarnieri, 090 2212289, rosalia.silvestri@unime.it
- Recruiting
Azienda Ospedaliero-Universitaria Pisana
Pisa
Enrica Bonanni, +39050992088, e.bonanni@med.unipi.it
- Recruiting
IRCCS Neuromed - Istituto Neurologico Mediterraneo
Pozzilli
Andrea Romigi, +3908659291, andrea.romigi@neuromed.it
- Not yet recruiting
Fondazione Policlinico Universitario Agostino Gemelli IRCCS
Roma
Valerio Brunetti, 0630154304, v.brunetti2509@gmail.com
- Not yet recruiting
Policlinico Tor Vergata
Roma
Claudio Liguori, +390620903132, dott.claudioliguori@yahoo.it
- Not yet recruiting
AOU Città della Salute e della Scienza di Torino - SC Otorinolaringoiatria
Torino
Giuseppe Riva, +393335865851, info@giusepperivaotorino.it
- Recruiting
USL Umbria1 - Ambulatorio disturbi del sonno
Umbertide
Chiara Bedetti, +390758935307, chiara.bedetti@uslumbria1.it
About this study
Obstructive Sleep Apnea (OSA) is the most common sleep-related breathing disorder, representing a major socioeconomic burden on healthcare systems worldwide. Studies performed in Europe in the last twenty years showed a very high prevalence and highlighted that the severity of untreated OSA worsens over time. OSA is associated also with an increased risk to develop cardiovascular, cerebrovascular and metabolic diseases. Finally, recent studies reported a very high mortality in untreated OSA patients, including those with mild severity.
Data on European population have been obtained by the "ESADA group" (European Sleep Apnea Database) , a consortium of 25 sleep center across Europe that includes three Italian Research Hospitals. The ESADA showed significant differences between European geographical macrozones in terms of symptoms and complications. However, no data are available for the Italian population in terms of prevalence, clinical presentation and comorbidities.
Read more
The present project aims to overcome this limitation by obtaining a more defined picture of OSA in Italy. A cohort study was designed in collaboration with the Sleep Centers endorsed by the Italian Scientific Society of Sleep Medicine (AIMS).
Aims of the present project are to:
- Assess the distribution different physiological (endotypes) and clinical patterns (phenotypes) of OSA in Italian patients
- Analyze the association between OSA and co-morbidities
- implementation of an "Italian database" for long-term follow-up studies.
Methods
- Clinical, sleep study and treatment data will be collected for each patient. A clinical questionnaire will be developed in order to standardize the clinical data collection; to this end a feasibility study will be performed on 100 patients (25 pts for Coordinator/HUB center).
- Excessive daytime Sleepiness, Neurocognitive, anxiety/depression screening
- A web-based data collection platform will be designed to store pseudo-anonymized individual data.
OUTCOMES
- Distribution of OSA severity in Italy according to the different classification methods
- Definition of metabolic, cerebro- and cardiovascular risk factors prevalence associated with OSA in Italian Population
- Distribution of different physiological and clinical patterns and their association with co-morbidities
- Definition of a screening/case finding questionnaire for Italian Population
- Definition of an ongoing cohort of patients that will be followed-up
- Implementation of an OSA registry that will be shared with Italian Health System or Agencies to designed preventive or early diagnosis interventions to reduce the health impact of the disease.
Read the detailed description
Obstructive Sleep Apnea (OSA) is the most common sleep-related breathing disorder, representing a major socioeconomic burden on healthcare systems worldwide. Studies performed in Europe in the last twenty years showed a very high prevalence and highlighted that the severity of untreated OSA worsens over time. OSA is associated also with an increased risk to develop cardiovascular, cerebrovascular and metabolic diseases. Finally, recent studies reported a very high mortality in untreated OSA patients, including those with mild severity.
Data on European population have been obtained by the "ESADA group" (European Sleep Apnea Database), a consortium of 25 sleep center across Europe that includes three Italian Research Hospitals. The ESADA showed significant differences between European geographical macrozones in terms of symptoms and complications. However, no data are available for the Italian population in terms of prevalence, clinical presentation and comorbidities.
The present project aims to overcome this limitation by obtaining a more defined picture of OSA in Italy. A cohort study was designed in collaboration with the Sleep Centers endorsed by the Italian Scientific Society of Sleep Medicine (AIMS).
Aims of the present project are to:
- Assess the distribution different physiological (endotypes) and clinical patterns (phenotypes) of OSA in Italian patients
- Analyze the association between OSA and co-morbidities by taking into account the phenotypes already described in the literature, i.e., ESADA, Icelandic Sleep Cohort, and BAVENO classification;
- implementation of an "Italian database" for long-term follow-up studies. The project will set an HUB and SPOKE organization that include 4 leading research Sleep Center distributed over the Italian territory in collaboration with the Italian Scientific Society of Sleep Medicine (AIMS) network. AIMS is member of the European Federation of National Sleep Society as well as part of World Sleep Association.
Methods
- Clinical, sleep study and treatment data will be collected for each patient. A clinical questionnaire will be developed in order to standardize the clinical data collection; to this end a feasibility study will be performed on 100 patients (25 pts for Coordinator/HUB center). Additional clinical tests will include: EKG, Spirometry, ABPM, standard blood chemistry, CPR, TSH reflex, glycemic control assesment, Vitamin D and B12.
- Excessive daytime Sleepiness, Neurocognitive, anxiety/depression screening will be performed by means of ESS, MOCA and HADS, respectively
- A web-based data collection platform will be designed to store pseudo-anonymized individual data.
OUTCOMES
- Distribution of OSA severity in Italy according to the different classification methods (AHI based; hypoxic burden; Icelandic Sleep Cohort, ESADA and BAVENO method)
- Definition of metabolic, cerebro- and cardiovascular risk factors prevalence associated with OSA in Italian Population
- Distribution of different physiological and clinical patterns and their association with co-morbidities; analysis of differences with other populations.
- Definition of a screening/case finding questionnaire for Italian Population
- Definition of an ongoing cohort of patients that will be followed-up
- Implementation of an OSA registry that will be shared with Italian Health System or Agencies to designed preventive or early diagnosis interventions to reduce the health impact of the disease.
- Conditions
- Sleep Apnea
- Being tested
- Polysomnography
- Keywords
- Sleep apnea, Phenotypes, Diagnosis
- Medical subject headings
- Sleep Apnea Syndromes, Disease
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
PolysomnographyDiagnostic test
Polysomnography after enrollment for suspected obstructive sleep apnea
| Study group | Role | What they receive |
|---|---|---|
| Patients with suspected obstructive sleep apnea (OSA) | Patients referred to the Italian Sleep Centres because of suspected OSA Receives: Diagnostic Test: Polysomnography |
What is being measured
The primary outcome is the main question the study is designed to answer.
Apnea-Hypopnea Index
Apnea-Hypopnea Index as determined by Polysomnography
Measured: At enrollment
Oxygen saturation
Oxygen saturation as determined by Polysomnography
Measured: At enrollment
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Mar 2025
- Study start1 Jun 2024
- Primary completion23 Oct 2025 (estimated)
- Study completion23 Oct 2025 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Sleep ApneaStudies of the same condition, open and under way.
- More trials run by Istituto Auxologico ItalianoThe sponsor's other registered studies.
- 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
- Cross-sectional
- Enrolment
- 5,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Istituto Auxologico Italiano
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06872242
- Sponsor's protocol ID
- 09M205
- Acronym
- IPNOS
- Status last verified
- Mar 2025
- First submitted
- 28 Feb 2025
- Last updated
- 12 Mar 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Study at a glance
From the registry record, last updated by the sponsor on 12 Mar 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Italian PheNotypes Obstructive Sleep Apnea Study
- ClinicalTrials.gov ID
- NCT06872242
- Acronym / sponsor ID
- IPNOS / 09M205
- Conditions
- Sleep Apnea
- Keywords
- Sleep apnea, Phenotypes, Diagnosis
- Study type
- Observational
- Recruitment status
- Recruiting
- Enrolment
- 5,000 participants (estimated)
- Lead sponsor
- Istituto Auxologico ItalianoUniversity, hospital or other
- Study start
- 1 Jun 2024 (actual)
- Primary completion
- 23 Oct 2025 (estimated)
- Study completion
- 23 Oct 2025 (estimated)
- First posted
- 12 Mar 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.
Obstructive Sleep Apnea (OSA) is the most common sleep-related breathing disorder, representing a major socioeconomic burden on healthcare systems worldwide. Studies performed in Europe in the last twenty years showed a very high prevalence and highlighted that the severity of untreated OSA worsens over time. OSA is associated also with an increased risk to develop cardiovascular, cerebrovascular and metabolic diseases. Finally, recent studies reported a very high mortality in untreated OSA patients, including those with mild severity.
Data on European population have been obtained by the "ESADA group" (European Sleep Apnea Database) , a consortium of 25 sleep center across Europe that includes three Italian Research Hospitals. The ESADA showed significant differences between European geographical macrozones in terms of symptoms and complications. However, no data are available for the Italian population in terms of prevalence, clinical presentation and comorbidities.
The present project aims to overcome this limitation by obtaining a more defined picture of OSA in Italy. A cohort study was designed in collaboration with the Sleep Centers endorsed by the Italian Scientific Society of Sleep Medicine (AIMS).
Aims of the present project are to:
- Assess the distribution different physiological (endotypes) and clinical patterns (phenotypes) of OSA in Italian patients
- Analyze the association between OSA and co-morbidities
- implementation of an "Italian database" for long-term follow-up studies.
Methods
- Clinical, sleep study and treatment data will be collected for each patient. A clinical questionnaire will be developed in order to standardize the clinical data collection; to this end a feasibility study will be performed on 100 patients (25 pts for Coordinator/HUB center).
- Excessive daytime Sleepiness, Neurocognitive, anxiety/depression screening
- A web-based data collection platform will be designed to store pseudo-anonymized individual data.
OUTCOMES
- Distribution of OSA severity in Italy according to the different classification methods
- Definition of metabolic, cerebro- and cardiovascular risk factors prevalence associated with OSA in Italian Population
- Distribution of different physiological and clinical patterns and their association with co-morbidities
- Definition of a screening/case finding questionnaire for Italian Population
- Definition of an ongoing cohort of patients that will be followed-up
- Implementation of an OSA registry that will be shared with Italian Health System or Agencies to designed preventive or early diagnosis interventions to reduce the health impact of the disease.
Detailed description
Obstructive Sleep Apnea (OSA) is the most common sleep-related breathing disorder, representing a major socioeconomic burden on healthcare systems worldwide. Studies performed in Europe in the last twenty years showed a very high prevalence and highlighted that the severity of untreated OSA worsens over time. OSA is associated also with an increased risk to develop cardiovascular, cerebrovascular and metabolic diseases. Finally, recent studies reported a very high mortality in untreated OSA patients, including those with mild severity.
Data on European population have been obtained by the "ESADA group" (European Sleep Apnea Database), a consortium of 25 sleep center across Europe that includes three Italian Research Hospitals. The ESADA showed significant differences between European geographical macrozones in terms of symptoms and complications. However, no data are available for the Italian population in terms of prevalence, clinical presentation and comorbidities.
The present project aims to overcome this limitation by obtaining a more defined picture of OSA in Italy. A cohort study was designed in collaboration with the Sleep Centers endorsed by the Italian Scientific Society of Sleep Medicine (AIMS).
Aims of the present project are to:
- Assess the distribution different physiological (endotypes) and clinical patterns (phenotypes) of OSA in Italian patients
- Analyze the association between OSA and co-morbidities by taking into account the phenotypes already described in the literature, i.e., ESADA, Icelandic Sleep Cohort, and BAVENO classification;
- implementation of an "Italian database" for long-term follow-up studies. The project will set an HUB and SPOKE organization that include 4 leading research Sleep Center distributed over the Italian territory in collaboration with the Italian Scientific Society of Sleep Medicine (AIMS) network. AIMS is member of the European Federation of National Sleep Society as well as part of World Sleep Association.
Methods
- Clinical, sleep study and treatment data will be collected for each patient. A clinical questionnaire will be developed in order to standardize the clinical data collection; to this end a feasibility study will be performed on 100 patients (25 pts for Coordinator/HUB center). Additional clinical tests will include: EKG, Spirometry, ABPM, standard blood chemistry, CPR, TSH reflex, glycemic control assesment, Vitamin D and B12.
- Excessive daytime Sleepiness, Neurocognitive, anxiety/depression screening will be performed by means of ESS, MOCA and HADS, respectively
- A web-based data collection platform will be designed to store pseudo-anonymized individual data.
OUTCOMES
- Distribution of OSA severity in Italy according to the different classification methods (AHI based; hypoxic burden; Icelandic Sleep Cohort, ESADA and BAVENO method)
- Definition of metabolic, cerebro- and cardiovascular risk factors prevalence associated with OSA in Italian Population
- Distribution of different physiological and clinical patterns and their association with co-morbidities; analysis of differences with other populations.
- Definition of a screening/case finding questionnaire for Italian Population
- Definition of an ongoing cohort of patients that will be followed-up
- Implementation of an OSA registry that will be shared with Italian Health System or Agencies to designed preventive or early diagnosis interventions to reduce the health impact of the disease.
Study design
- Observational model
- Cohort
- Time perspective
- Cross-sectional
- Number of arms
- 1
| Arm | Type | Receives |
|---|---|---|
| Patients with suspected obstructive sleep apnea (OSA) | – | Diagnostic Test: PolysomnographyPatients referred to the Italian Sleep Centres because of suspected OSA |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Age groups
- Adult, Older adult
- Study population
- Adult patients referred to the Italian Sleep Centres because of suspected Obstructive Sleep Apnea
Key inclusion criteria (2 listed)
- Suspected Obstructive Sleep Apnea
- Age 18 years or older
Key exclusion criteria (2 listed)
- Unstable psychiatric disease
- Limited life expectancy due to illness unrelated to sleep apnoea or other medical conditions which may interfere with the study protocol in the opinion of the investigator
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 |
|---|---|---|
| PolysomnographyPolysomnography after enrollment for suspected obstructive sleep apnea | Diagnostic test | Patients with suspected obstructive sleep apnea (OSA) |
Primary outcome
Apnea-Hypopnea Index
Time frame: At enrollment
Apnea-Hypopnea Index as determined by Polysomnography
Oxygen saturation
Time frame: At enrollment
Oxygen saturation as determined by Polysomnography
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Mar 2025.
- Individual participant dataSharing planned: No
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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.
30 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
An observational study of Sleep Apnea, run by Istituto Auxologico Italiano at 30 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 2 inclusion and 2 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: looking for participants now, as of the sponsor's last update on 12 Mar 2025. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 30 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?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Carolina Lombardi, PhD (+3902619111 ext. 2750, c.lombardi@auxologico.it), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Apnea-Hypopnea Index (time frame: At enrollment). The study lists 2 primary outcomes in all. 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 12 Mar 2025.