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NCT07274176

The Effect of Graded Forced Expiration on Intraocular Pressure

Recruiting now NA Last updated 22 December 2025
What this trial tests

NA trial testing Intraocular Pressure after forced expiration in Intraocular Pressure in 60 participants. Currently enrolling.

Timeline
15 December 2025
Primary endpoint
10 February 2026
25 February 2026

Quick facts

Lead sponsorUşak University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposescreening
Enrollment60
Start date15 December 2025
Primary completion10 February 2026
Estimated completion25 February 2026
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Uşak University

Who can join

Adults 18 to 65, any sex, with Intraocular Pressure. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Intraocular Pressure

Currently open trials in the same condition.

Other Uşak University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07274176.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing