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Not Yet RecruitingNCT07177131

Hydration Status and Ocular Parameters Study

Prospective, Randomized Cross-over Within-subject Study on the Effects of Dehydration and Hyperhydration on Macular Thickness, Corneal Morphology, and Ocular Biometric Parameters Measured by OCT, Pentacam and Optical Biometer

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
60 (estimated)
Sponsor
Ante Kreso · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study will examine how hydration status (drinking a large amount of water or avoiding water for a short period of time) affects the eye. Healthy adult volunteers will participate in two sessions: one after mild dehydration (no water for 12 hours) and one after drinking 2 liters of water within 4 hours. At each session, detailed eye measurements will be taken, including scans of the retina and optic nerve using optical coherence tomography (OCT), corneal imaging with Pentacam, and eye length measurements with an optical biometer. The results from the two conditions will be compared within the same participants. The main goal is to determine whether hydration influences the thickness of the retina (macula). Secondary goals include assessing changes in the optic nerve, cornea, and other biometric eye parameters. The study involves only non-invasive tests and minimal risk. Findings may help improve understanding of how hydration affects the eye and may be important for clinical practice, such as planning cataract or refractive surgery.

Conditions

Interventions

TypeNameDescription
BEHAVIORALRelative Dehydration ProtocolParticipants will abstain from water intake for 12 hours prior to the study visit. Food is allowed, but fluid intake is limited to a maximum of 250 ml until 20:00 h on the previous evening. Eye measurements will be performed in the morning (8-10 h).
BEHAVIORALHyperhydration ProtocolParticipants will consume 2 liters of water within 4 hours prior to the study visit. Eye measurements will be performed in the morning (8-10 h).

Timeline

Start date
2025-09-25
Primary completion
2025-11-01
Completion
2025-12-01
First posted
2025-09-16
Last updated
2025-09-22

Source: ClinicalTrials.gov record NCT07177131. Inclusion in this directory is not an endorsement.