MicroRNAs as Biomarkers for Obstructive Sleep Apnea
Launched by UNIVERSITY OF PENNSYLVANIA · Dec 19, 2023
Trial Information
Current as of July 23, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial is studying a condition called obstructive sleep apnea (OSA), which is a common sleep disorder that affects breathing during sleep. The goal of the study is to find specific markers in the blood, known as microRNAs, that can help identify OSA patients, track how well treatments are working, and predict how treatment might affect blood pressure. Currently, there are no easy blood tests to diagnose or manage OSA, so this research could lead to important advancements in patient care.
To participate in the trial, individuals need to be between 18 and 75 years old. Those with moderate to severe OSA (having 15 or more breathing events per hour during sleep) and who are willing to use a CPAP machine (a common treatment) may be eligible. On the other hand, healthy participants without OSA (fewer than 5 events per hour) are also needed for comparison. It's important to note that those currently using OSA treatments or with certain health conditions, like severe kidney disease, cannot participate. Participants can expect to provide blood samples and undergo assessments to help researchers understand how these microRNAs relate to OSA.
Gender
ALL
Eligibility criteria
- Inclusion Criteria for Cases:
- • age 18-75 years
- • moderate-severe OSA (defined as AHI ≥15 events/hour)
- • willing to accept PAP therapy
- Inclusion Criteria for Controls:
- • age 18-75 years
- • no OSA (defined as AHI \<5 events/hour)
- Exclusion Criteria for Cases:
- • current use of PAP or other OSA treatments
- • home oxygen therapy
- • recent changes (within 3 months) to BP medications among those who are on these medications
- • presence of Cheyne-Stokes Respiration (CSR) in sleep study
- • predominantly central sleep apnea (AHI≥15 events/hour, with \>50% central events)
- • pregnancy
- • clinical history of chronic kidney disease (Stage 5) requiring dialysis, or renal transplant
- • organ transplantation
- • self-reported sleep duration less than 5 hours per night on weeknights (work nights)
- • current night shift work
- Exclusion Criteria for Controls:
- • home oxygen therapy
- • pregnancy
- • clinical history of chronic kidney disease (Stage 5) requiring dialysis, or renal transplant
- • organ transplantation
- • self-reported sleep duration less than 5 hours per night on weeknights (work nights)
- • current night shift work
About University Of Pennsylvania
The University of Pennsylvania, a prestigious Ivy League institution located in Philadelphia, is renowned for its commitment to advancing medical research and improving healthcare outcomes. As a clinical trial sponsor, the university leverages its extensive resources, interdisciplinary expertise, and cutting-edge facilities to conduct innovative studies across various therapeutic areas. With a focus on translating scientific discoveries into clinical applications, the University of Pennsylvania fosters collaborations among leading researchers, clinicians, and industry partners, ensuring rigorous trial design and adherence to ethical standards. Through its dedication to excellence in research and education, the university plays a pivotal role in shaping the future of medicine.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Philadelphia, Pennsylvania, United States
Reykjavík, , Iceland
Columbus, Ohio, United States
Patients applied
Trial Officials
Allan I Pack, MBChB, PhD
Principal Investigator
University of Pennsylvania
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported