Sleep Apnea, Obstructive Clinical Trial
Official title:
The Benefit of a Liraglutide-based Weight Management Alone or in Addition to Standard CPAP Therapy on Metabolic Function in Patients With Obstructive Sleep Apnoea (OSA) - an Explorative, Proof-of-concept Study
NCT number | NCT04186494 |
Other study ID # | RS19-023 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | December 2, 2019 |
Est. completion date | July 31, 2022 |
Verified date | December 2023 |
Source | St Vincent's University Hospital, Ireland |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This is an explorative, proof-of-concept study exploring the potential therapeutic role of a Liraglutide-based weight loss regimen versus standard CPAP or the combination of both on metabolic parameters, blood pressure, endothelial function, coronary artery calcification, vascular inflammation and apnea/hypopnea index in non-diabetic patients with moderate to severe obstructive sleep apnea
Status | Completed |
Enrollment | 30 |
Est. completion date | July 31, 2022 |
Est. primary completion date | December 31, 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 60 Years |
Eligibility | Inclusion Criteria: - Newly diagnosed moderate-severe OSA (by standard PSG) - Body mass index between 30 - 40 - Age 18 - 60 years - Able to provide written, informed consent Exclusion Criteria: - Pregnancy - Requirement for supplemental oxygen - Previous diagnosis of OSA or previous CPAP treatment - Diagnosis of Diabetes - Previous treatment with GLP-1 analogue - Previous surgical treatment for obesity - Active treatment for malignancy or severe psychiatric disorder - Acute coronary syndrome or stroke within 3 months prior to study - History of decompensated heart failure - Professional drivers or drivers with a history of road-traffic accident due to sleepiness - Severe excessive daytime sleepiness defined as Epworth sleepiness scale >15 |
Country | Name | City | State |
---|---|---|---|
Ireland | St Vincent's University Hospital | Dublin | Dublin 4 |
Lead Sponsor | Collaborator |
---|---|
St Vincent's University Hospital, Ireland | Health Research Board, Ireland, University College Dublin |
Ireland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Insulin resistance | Improvement in insulin resistance defined by HOMA-IR | 6 months | |
Secondary | Weight | Change in body mass index | 6 months | |
Secondary | Glucose tolerance | Change in glucose tolerance measured by oral glucose tolerance test | 6 months | |
Secondary | OSA Severity | Change in apnea/hypopnea index as per polysomnography | 6 months | |
Secondary | Blood pressure | Change in 24-hour blood pressure | 6 months | |
Secondary | Endothelial function | Change in microvascular endothelial function measured by EndoPat | 6 months | |
Secondary | Coronary artery calcification | Change in coronary artery calcification score determined by Coronary artery CT | 6 months | |
Secondary | Vascular inflammation | Change in vascular inflammation determined via FDG-PET scan | 6 months |
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