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Comparing Diurnal Fluctuations in Intra Ocular Pressure Measured in Same Day Versus Different Days in Glaucoma Patients (IOP)

I

Israel Healthcare Foundation

Status

Completed

Conditions

Glaucoma

Study type

Observational

Funder types

Other

Identifiers

NCT01709916
CMC-11-0037-CTIL

Details and patient eligibility

About

Glaucoma is one of the leading causes of blindness in the west. The disease caused by high intra ocular pressure (IOP) and characterized by damage to the optic nerve and gradual loss of visual field. Intra ocular pressure change during the day. To evaluate the efficiency of the therapy it is common to measure the intra ocular pressure at different times of the day. Most ophthalmologists admit the patient for one day at which intra ocular pressure is measured at different times. This method does not mimic the patient daily routine and may not reflect the true diurnal fluctuations.

For this reason some ophthalmologists measure the intra ocular pressure at different times and at different days. It is not known if both methods give similar diurnal curves.

Full description

A study physician will install anesthetic eye drops and will color the eye drops film with fluorescein. Study physician will use tonometer to measure the intra ocular pressure in each eye. This is a standard procedure done in any ophthalmological examination. Each patient will undergo intraocular pressure examination at 8:00, 12:00 and 16:00.

In the first day intra ocular pressure will be measured at 8:00, 12:00 and 16:00, same day measurements. The day after intra ocular pressure will be measured at 8:00, two days after at 12:00 and three days after at 16:00. One month later the patient will undergo another serious of intra ocular pressure measurements.

In the first day intra ocular pressure will be measured at 8:00, 12:00 and 16:00, same day measurements. The day after intra ocular pressure will be measured at 8:00, two days after at 12:00 and three days after at 16:00.

The relationship between the two diurnal curves will be analyzed.

Enrollment

50 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Glaucoma patient.
  • Age 18-80 years
  • Able to read and understand Hebrew, able to sign informed consent in Hebrew.

Exclusion criteria

  • Ophthalmic laser treatment or surgery 3 months prior to enrollment.
  • Eye infection or inflammation.
  • Corneal pathology altering IOP measurement.
  • Patients not cooperating during IOP measurement.
  • non compliant patients

Trial design

50 participants in 1 patient group

Glaucoma patients
Description:
Glaucoma patients treated with eye drops to lower the IOP.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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