Clinical Trial

The Effect of Graded Forced Expiration on Intraocular Pressure

Completed
View on ClinicalTrials.gov →
Summary
The primary objective of this study is to utilize the Airofit device to systematically measure and characterize the changes in intraocular pressure across its six different levels of forced expiration. This investigation will provide crucial quantitative data on the IOP-respiratory effort relationship, enhancing our understanding of IOP dynamics during controlled respiratory stress and establishing a new, standardized paradigm for such research.
Protocol Amendment History 2 amendments
This ClinicalTrials.gov record has been amended 2 times since 2025-11-27; most recent amendment 2026-07-17.
Status change: Recruiting → Completed 2026-07-17
Trial Details
NCT Number NCT07274176
Lead Sponsor Uşak University
Conditions Intraocular Pressure
Enrollment 60 participants
Start Date 2025-12-15
Primary Completion 2026-02-10 (estimated)
Study Completion 2026-03-25 (estimated)
Updated on ClinicalTrials.gov 2026-07-20