ClinicalTrials.gg
Enrolling by invitationNCT05890911Updated Aug 31, 2026

The Meaning of Dopaminergic Pathway in Sleep Breathing Disorders.

An observational study in Sleep Apnea and Sleep-Disordered Breathing, sponsored by Wroclaw Medical University. Enrolling by invitation at 1 site in Poland. Open to participants aged 18 Years to 80 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-31.

Sponsored by Wroclaw Medical University · Observational

Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
100
Ages
18 Years to 80 Years
Sex
All
01

Study summary

The participants in the study will be adult patients with suspected sleep-disordered breathing. A one-night polysomnography will be performed using the NOXA1 device (NOX Medical, Reykjavík, Iceland). During the polysomnographic examination, sleep, breathing, heart rate and activity of the masticatory muscles will be recorded. Blood sample will be taken from each of the participants qualified to the study and control group to determine the level of dopamine and used to perform genetic tests of selected single nucleotide polymorphisms occurring within the genes regulating the concentration of dopamine and genes encoding dopamine receptors.

Read the detailed description

Sleep-disordered breathing (SDB) refers to a spectrum of abnormalities related to sleep. Obstructive sleep apnea (OSA) is the most common type of SDB and affects approximately one billion adults worldwide. Untreated OSA leads to significant comorbidities and increased mortality due to significantly increased risk of stroke and heart attack. Because of limited access to objective sleep studies and the fact that untreated OSA is a real risk factor premature death, the determination of possible organic reasons for its occurrence is a key aspect. The purpose of the study is to determine the importance of dopamine levels and selected single nucleotide polymorphisms within genes regulating the concentration of dopamine - the gene responsible for production of the enzyme catechol-O-methyltransferase (COMT) - rs4680 and rs6269 and genes encoding receptors dopamine (DRD1 - rs686, rs5327 and DRD2 - rs1800497) in assessment of the risk of development and advancement of SDB. The participants of the study will be adult patients hospitalized in the Department of Internal Diseases, Occupational Diseases, Hypertension and Clinical Oncology of the Wroclaw Medical University due to suspicion of SDB. One-night polysomnography study will be performed using the NOXA1 device (NOX Medical, Reykjavík, Iceland) at the Sleep Laboratory. During the examination parameters regarding sleep, breathing, heart rate and activity of the masticatory muscles will be recorded. The study group will consist of the participants in whom, on the basis of 3rd edition of the International Classification of Sleep Disorders of the American Academy of Sleep Medicine SDB will be recognized. Control group will consist of healthy participants matched in terms of age and sex. A blood sample will be collected from all participants to determine the level of dopamine and to perform genetic test of selected single nucleotide polymorphisms within the genes regulating the concentration of dopamine - the gene responsible for production the enzyme catechol-O-methyltransferase (COMT) - rs4680 and rs6269 and genes encoding dopamine receptors (DRD1 - rs686, rs5327 and DRD2 - rs1800497). Study group and control group will be compared and the results will be statistically analysed.

02

Conditions studied

  • Sleep Apnea
  • Sleep-Disordered Breathing

Keywords

  • sleep apnea
  • sleep-disordered breathing
  • sleep disorder
  • dopamine
03

In context

Sleep Apnea Syndromes

1,084 studies on the registry are indexed under Sleep Apnea Syndromes; 171 are open to participants now.

This study's planned enrollment of 100 is below the median of 150 across 343 observational studies indexed under Sleep Apnea Syndromes.

Browse Sleep Apnea Syndromes studies →

Lead sponsor

Wroclaw Medical University is the lead sponsor of 99 studies on the registry; 29 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years to 80 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Probability sample

Study population

Patients with suspicion of sleep-disordered breathing referred to the Department of Internal Medicine, Occupational Diseases, Hypertension and Clinical Oncology operating at the Wroclaw Medical University. Healthy controls.

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

  • age between 18 and 80 years old
  • suspicion of sleep-disordered breathing

Exclusion criteria

Exclusion Criteria:

  • age under 18
  • age over 80
  • severe disorders and systemic diseases (including genetical disorders)
  • neurological disorders
  • active inflammations
  • active cancer
  • severe mental disorders and retardation (including genetical)
  • taking drugs that could falsify polysomnography
  • confirmed alcoholism
  • drug addiction
  • pregnancy and breast feeding
  • treatment using or dependence on any painkillers and/or drugs and substances that may affect nervous, muscular and respiratory system functions
  • lack of consent to participate in the study
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
100 participants (estimated)
Patient registry
No
Biospecimen retention
Samples with dna

Groups and cohorts

  • Study group

    Participants with the diagnosis of sleep-disordered breathing

    Diagnostic Test: Polysomnography · Diagnostic Test: Blood dopamine level measurement · Diagnostic Test: Genetical test

  • Control group

    Healthy participants without diagnosis of sleep-disordered breathing

    Diagnostic Test: Polysomnography · Diagnostic Test: Blood dopamine level measurement · Diagnostic Test: Genetical test

Interventions

  • Diagnostic testPolysomnography

    Each of the patients will undergo polysomnography

  • Diagnostic testBlood dopamine level measurement

    In each of the patients blood dopamine level will be measured

  • Diagnostic testGenetical test

    Each of the patients will undergo genetical test focusing on selected single nucleotide polymorphisms within genes regulating the concentration of dopamine - the gene responsible for production of the enzyme catechol-O-methyltransferase (COMT) - rs4680 and rs6269 and genes encoding receptors dopamine (DRD1 - rs686, rs5327 and DRD2 - rs1800497).

06

What researchers measure

Primary outcomes

  1. Relationship between sleep-disordered breathing and blood dopamine level.

    Each participant will undergo blood test focusing on the level of dopamine.

    Time frame: June 1, 2023 - December 31, 2023

Secondary outcomes

  1. Relationship between sleep-disordered breathing and polymorphism within genes regulating the concentration and encoding receptors of dopamine.

    Each participant will undergo genetical blood test focusing on the polymorphisms within genes regulating the concentration of dopamine - the gene responsible for production of the enzyme catechol-O-methyltransferase (COMT) - rs4680 and rs6269 and genes encoding receptors dopamine (DRD1 - rs686, rs5327 and DRD2 - rs1800497).

    Time frame: June 1, 2023 - December 31, 2023

  2. Relationship between sleep bruxism and blood dopamine level.

    Each participant will undergo blood test focusing on the level of dopamine.

    Time frame: June 1, 2023 - December 31, 2023

  3. Relationship between sleep bruxism and polymorphism within genes regulating the concentration and encoding receptors of dopamine.

    Each participant will undergo genetical blood test focusing on the polymorphisms within genes regulating the concentration of dopamine - the gene responsible for production of the enzyme catechol-O-methyltransferase (COMT) - rs4680 and rs6269 and genes encoding receptors dopamine (DRD1 - rs686, rs5327 and DRD2 - rs1800497).

    Time frame: June 1, 2023 - December 31, 2023

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Aug 31, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT05890911
Lead sponsor
Wroclaw Medical University
Responsible party
Joanna Smardz (Principal Investigator, Wroclaw Medical University) — Principal investigator
First posted
Jun 6, 2023
Start date
Jun 1, 2023
Primary completion
Dec 2026 (estimated)
Completion
Dec 2026 (estimated)
Last update
Aug 31, 2026

Study contacts

Joanna Smardz, Ph.D
principal investigator · Wroclaw Medical University

Oversight

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

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

No contact was published for this record. The registry link below has the sponsor’s details.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion