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The Effect of Body Posture on Intraocular Pressure in Progressive Glaucoma

The Effect of Body Posture on Intraocular Pressure in Progressive Glaucoma

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01351779
Enrollment
20
Registered
2011-05-11
Start date
2011-05-31
Completion date
Unknown
Last updated
2011-05-11

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

Conditions

Glaucoma

Keywords

Intraocular pressure, Contact lens sensor, Optic disc hemorrhage

Brief summary

Glaucoma is a condition where the optic nerve (the nerve responsible for sight) shows progressive damage with characteristic loss of visual field. Glaucoma is very commonly associated with raised pressure in the eye (intraocular pressure \[IOP\]). IOP has been shown to increase when lying down in normal subjects as well as patients with glaucoma. It is possible that this effect can make glaucoma worse. This study is designed to investigate the effect of body posture (particularly when sleeping) on the IOP fluctuation in the eye. Each patient will be required to attend for 2 separate 24 hour visits. On one visit the patient will be required to sleep flat and on the other visit at a 30° head up sleeping position. During this time the patient will be required to wear a soft contact lens (SENSIMED Triggerfish®) which has a special sensor on it that monitors the IOP continuously. The IOP measurements are wirelessly transmitted to a recorder.

Interventions

None listed

Sponsors

Sensimed AG
CollaboratorINDUSTRY
University of Toronto
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* signed informed consent * diagnosis of primary open angle glaucoma (POAG) or normal tension glaucoma (NTG) that is progressing based on recent or recurrent optic disc hemorrhage * age 18-85 years * not more than 4 diopters of spherical equivalent or 2 diopters of cylinder equivalent in study eye * stable anti-glaucoma treatment for 4 weeks before first session * for women of childbearing potential, adequate contraception

Exclusion criteria

* unwilling or unable to sleep in a flat or 30 degrees head up position * ocular surgery in previous 3 months * corneal or conjunctival abnormality * wear of full frame metallic glasses during monitoring session * severe dry eye * secondary forms of glaucoma * allergy to corneal anaesthesia * patients with contraindications for contact lens wear * pregnancy and lactation * patients unable to understand the character and individual consequences of the investigation * simultaneous participation in other research

Design outcomes

Primary

MeasureTime frameDescription
Intraocular pressure changes that occur during sleep and with changes in body posture24 hoursThe intraocular pressure will be continuously monitored with a wireless contact lens sensor device over a 24 hour period

Secondary

MeasureTime frameDescription
Incidence of side effects or adverse effects that occur while subjects are wearing the contact lens device24 hoursPatients will be monitored for contact lens related side effects or adverse effects that occur during the monitoring session.

Countries

Canada

Contacts

Primary ContactGraham Prof Trope, PhD, FRCSC
Graham.Trope@uhn.on.ca4166035317
Backup ContactYvonne Prof Buys, MD, FRCSC
y.buys@utoronta.ca4166035682

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026