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Water Drinking Test Study and Disc Hemorrhages in Normal Tension Glaucoma

Correlation Between Water Drinking Test Study and Disc Hemorrhages in Normal Tension Glaucoma

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05075369
Enrollment
20
Registered
2021-10-12
Start date
2021-10-31
Completion date
2022-04-30
Last updated
2021-10-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Normal Tension Glaucoma

Keywords

normal tension glaucoma, disc hemorrhages, water drinking test

Brief summary

Disc hemorrhages are a known risk factor for progression of glaucoma. A positive water drinking test is also associated with progression of primary open glaucoma. The purpose of this study is to determine if patients with normal tension glaucoma and disc hemorrhages have a positive water drinking test. Patients with normal tension glaucoma and a disc hemorrhage will be recruited to undergo a water drinking test prior to any change in their treatment.

Detailed description

Patient with normal tension glaucoma under the care of a fellowship trained glaucoma specialist and noted to have a disc hemorrhage in one or both eyes when examined in the office will be recruited to undergo a water drinking test (WDT). After an informed consent is obtained, arrangements will be made to undergo the WDT either at the ophthalmologist's office or the local hospital clinic(Misericordia). The test will be administered in the following way: Upon arrival the patients baseline intraocular pressure (IOP) will be measured, then shortly afterwards the patient will drink 800 ml of water in a period of 5 minutes. Immediately after the water ingestion has finished a second IOP will be measured, followed by IOP measurements every 15 minutes for 60 minutes with a Goldman applanation tonometer by the same examiner. All of these measurements will be collected in a data sheet for the WTD. A total of 60 minutes would be the duration of the activity.

Interventions

DIAGNOSTIC_TESTwater drinking test

Water drinking test-glaucoma diagnostic test - marker for outflow facility reserve to detect IOP instability when the body ingests 800 ml of water within a 5 minute period of time

Sponsors

University of Manitoba
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Intervention model description

patients with a diagnosis of normal tension glaucoma and noted to have a disc hemorrhage

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis of normal tension glaucoma by a fellowship trained glaucoma specialist, * Clinical diagnosis of a disc hemorrhage diagnosed by a fellowship trained glaucoma specialist, * Must be able to swallow water * Must be able to be positioned to allow accurate measurement of the Intraocular pressure with a slit lamp mounted Goldmann applanation tonometer * Must have a smooth corneal surface to allow for accurate Goldmann application tonometry measurement * Outpatient * A sufficient level of education to understand study procedures and be able to communicate with site personnel

Exclusion criteria

* History of refractive surgery, * Active ocular infection, * Pregnancy, * Cardiac or renal diseases, history of urinary retention, * Corneal abnormalities preventing reliable IOP measurements, * Previous trabeculectomy or glaucoma shunt surgery, * Previous laser iridotomy, * Cognitive impairment or language barrier preventing ability to provide an informed consent.

Design outcomes

Primary

MeasureTime frameDescription
Change in baseline intraocular pressure(IOP) with water drinking testThe water drinking test takes 60 minutes, and the participant is then finished and can leave.The change in intraocular pressure in patients with normal tension glaucoma and a disc hemorrhage after undergoing the water drinking test will be measured with Goldmann applanation tonometry. A change from baseline IOP of 5 mm Hg is considered abnormal .

Contacts

Primary ContactLisa Gould, MD, FRCS
lisa.gould@umanitoba.ca204-957-3252
Backup ContactKarla Zuniga, MD
kzunigak@gmail.com204-583-2762

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026