Could a blood protein reveal hidden heart risks in sleep apnea?
NCT ID NCT07829809
First seen Sep 21, 2026 · Last updated Sep 21, 2026
Summary
Researchers are studying whether a blood protein called adropin can signal blood vessel damage and disease severity in obese adults with obstructive sleep apnea. The trial compares adropin levels in obese patients with and without the sleep disorder, and checks how those levels relate to breathing pauses during sleep and to a marker of vessel dysfunction called endothelin-1. About 80 adults aged 20 to 75 provide fasting blood samples after a sleep study. The goal is to see whether adropin could serve as an early warning sign for cardiovascular problems in this group.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a blood test for adropin, a protein measured in fasting blood samples
- What this could lead to
- If adropin tracks with blood vessel damage in sleep apnea, doctors could one day use a simple blood test to spot heart and vessel risks earlier in obese patients with the condition.
- What could go wrong
- This is a small observational study of 80 people at a single center, so it can only show associations, not cause and effect. Adropin levels may not reliably predict vessel problems, and the findings may not apply to other groups.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 80 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Sep 2026
An estimate. Start dates often move.
- Expected to finish
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Oct 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study will include adult obese participants who are referred to the Sleep Medicine/Chest outpatient clinic with suspected obstructive sleep apnea. Participants will undergo clinical assessment and overnight polysomnography (PSG) to confirm the diagnosis of OSA and determine its severity according to the apnea-hypopnea index (AHI). Participants will be categorized into appropriate study groups according to the presence and severity of OSA. A suitable comparison group of obese participants without OSA may also be included, according to the study design. The study population will include both males and females who meet the predefined inclusion criteria and provide informed consent to participate in the study
- Ages
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20 to 75 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * 1- Adults aged 20-75 years. 2-obese Patients diagnosed with obstructive sleep apnea (OSA) confirmed by polysomnography. 3- Patients willing to provide written informed consent. 4- Patients not currently on medications affecting endothelial function (e.g., statins, ACE inhibitors) or able to temporarily withhold under medical supervision. 5- Ability to comply with study procedures and follow-up Exclusion Criteria: * 1-Pregnant females 2-Thyroid disorders 3-Autoimmune diseases 4-chronic liver disease 5-chronic kidney disease 6-drugs as statin,glucocorticoids and antidepressant
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
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