← Trials/Trial dossier/NCT07281196
Semaglutide Effects on Sleep Apnea in Patients With Type 2 Diabetes/Obesity and Comorbid Obstructive Sleep Apnea
A Real-World Study on Changes in Sleep Apnea Among Patients With Type 2 Diabetes/Obesity and Comorbid OSA After Short-Term Treatment With Semaglutide
Lead sponsor
Assets
GLP-1 / incretin class catch-all / Semaglutide
Listed sites
1
Recruiting sites
—
Enrollment
15
actual
Study population
Obesity / overweight, Sleep apnea
Key I/E criterion
•BMI ≥27
Primary endpoint
•AHI, change
Footprint
Where this trial recruits
Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
Study population text
15 adults with T2DM/obesity and OSA receiving semaglutide
Eligibility criteria
1. Age 18-65 years. 2. BMI ≥27 kg/m²,with ≥1 comorbidity (hypertension, dyslipidemia, CVD) or T2DM. 3. On the basis of dietary control and exercise, the therapeutic effect is not satisfactory. There are indications for the use of semaglutide in clinical practice.
4. Combined with obstructive sleep apnea syndrome. 5. Within the past month, no hormone drug treatment that affects glucose and lipid metabolism, nor any drugs such as antibiotics that significantly interfere with the oral flora, or bariatric surgery has been received.
6. With complete information for this study. Exclusion Criteria.
1. Abnormal weight gain caused by endocrine diseases (pituitary/adrenal diseases, such as Cushing's syndrome; Or hypothyroidism, etc.)
2. Severe renal/hepatic impairment (eGFR <45 mL/min; ALT/AST >2.5×ULN).
3. Severe metabolic diseases, such as diabetic ketoacidosis and hyperosmolar hyperglycemic state, etc.
4. Patients with type 1 diabetes or other special types of diabetes, patients with type 2 diabetes with severely impaired pancreatic islet function, or patients with type 2 diabetes who use insulin.
5. There is a known history of drug use that affects glycolipid metabolism within three months, such as ① glucocorticoids; ② Fluoroquinolone antibiotics; ③ Beta-blockers such as metoprolol, etc. ④ Thyroid preparations such as thyroid hormone tablets; ⑤ Psychotropic drugs, including antipsychotic drugs such as chlorpromazine and olanzapine, as well as anti-anxiety or anti-depression drugs like SSRIS and NaSSAs; ⑥ SABA bronchodilators such as salbutamol and terbutaline; ⑦ Other known drugs that affect glycolipid metabolism, such as statins.
6. Severe bleeding tendency, urinary and reproductive system infections; There are contraindications for the use of semaglutide, such as a history of acute or chronic pancreatitis, medullary thyroid carcinoma, and multiple endocrine neoplasia (MEN) type 2.
7. Patients with contraindications to radiological examinations.
8. Patients with advanced malignant tumors.
9. Severe cardiovascular and cerebrovascular diseases, such as heart failure, etc.
10. Rheumatic immune diseases, etc.
11. Pregnant women and lactating women.
12. Patients who have taken or are currently taking diuretics such as loop diuretics and thiazides within the past month.
13. Currently involved in other interventional researchers.
14. Other situations that the researchers consider unsuitable for the study, such as poor compliance, etc.
Endpoints (9)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Coverage by outcome category
Weight & body composition
3 endpointsChanges in BMI
Time frame:Baseline, 1 week, 4 weeks
BMI, change
change from baseline, improvement
Changes in weight
Time frame:Baseline, 1 week, 4 weeks
Body weight, absolute change (kg)
change from baseline, improvement
Changes in waist circumference
Time frame:Baseline, 1 week, 4 weeks
Waist circumference, change
change from baseline, improvement
Glycemic / diabetes
1 endpointChanges in fasting glucose
Time frame:Baseline, 1 week, 4 weeks
Fasting glucose, change
change from baseline, improvement
LOINC 1558-6
MASH / liver
1 endpointChanges in liver enzymes
Time frame:Baseline, 1 week, 4 weeks
change from baseline, improvement
Cardiometabolic biomarkers
2 endpointsChanges in blood pressure
Time frame:Baseline, 1 week, 4 weeks
change from baseline, improvement
Changes in lipid profiles
Time frame:Baseline, 1 week, 4 weeks
change from baseline, improvement
Other clinical outcomes
1 endpointChanges in Apnea-Hypopea Index (AHI)
Time frame:Baseline and 1 week
AHI, change
change from baseline, improvement
Other (unclassified)
1 endpointChanges in glycated albumin
Time frame:Baseline, 1 week, 4 weeks
change from baseline, improvement
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.