Relationship Between 24-hour IOP Pattern and the 24-hour Blood Pressure Pattern in Patients With POAG
- Conditions
- Normal Tension GlaucomaPrimary Open Angle Glaucoma
- Interventions
- Device: Sensimed Triggerfish®
- Registration Number
- NCT01769521
- Lead Sponsor
- Sensimed AG
- Brief Summary
Interplay between the increasing IOP and decreasing blood pressure (BP) during the 24-hour period, especially in the nocturnal period, may lead to insufficient perfusion pressure of the optic nerve and contribute to the glaucomatous damage in adjunct to the antero-posterior vectorial mechanical impact on the lamina cribrosa, the translaminar pressure. Patients with progressive VF loss showed greater nocturnal BP dips than patients with stable VF. Reduced mean intraocular perfusion pressure (IOPP) was significantly associated with the extent of glaucomatous damage. How the nycthemeral IOP fluctuation influences glaucoma progression has not been studied in a prospective manner and remains to be elucidated.
The purpose of this study is to assess the relationship between the 24-hour IOP fluctuation pattern and the 24-hour BP pattern in patients with primary open angle glaucoma (POAG). IOP fluctuations will be monitored with SENSIMED Triggerfish®, a portable investigational device using a contact lens sensor that monitors the IOP fluctuation continuously over 24-hours.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 20
- Diagnosis of POAG, including progressing normal tension glaucoma (NTG) based on recent or recurrent disc haemorrhage
- No anti-glaucomatous drug treatment or washed-out for a period of 4 weeks prior to SD0 and absent throughout the study
- Aged more than 18 years, of either sex
- Not more than 4 diopters spherical equivalent on both eyes
- Not more than 2 diopters cylinder equivalent on both eyes
- Have given written informed consent, prior to pre-study screening
- Patients with history of ocular surgery within the last 3 months
- Corneal or conjunctival abnormality hindering contact lens adaptation
- Severe dry eye
- Secondary forms of OAG
- Patients with systemic hypertension
- Patients with allergy to corneal anesthetic
- Patients with contraindications for silicone contact lens wear
- Wear of full frame metallic glasses during Triggerfish® monitoring
- Patients not able to understand the character and individual consequences of the investigation
- Simultaneous participation in other clinical research
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Triggerfish Sensimed Triggerfish® Device: Sensimed Triggerfish
- Primary Outcome Measures
Name Time Method To evaluate the relationship between the 24-hour IOP fluctuations as monitored by Triggerfish® and the 24-hour blood pressure pattern in patients with POAG. 24-hour
- Secondary Outcome Measures
Name Time Method Relationship between the nocturnal IOP fluctuation pattern and the diurnal fluctuation pattern (office hours) 24 hours The nocturnal IOP fluctuation pattern will be compared to that of the diurnal fluctuation pattern (office hours). The diurnal IOP fluctuation pattern will be compared to the tonometric IOP curve concomitantly assessed in the contralateral eye.
Relationship between the intraocular pulsation frequency and heart rate (HR) 24-hours The relationship between the intraocular pulsation frequency as determined by Triggerfish® will be correlated with the heart frequency as determined by ECG
Nycthemeral IOP pattern 24-hour The nycthemeral IOP fluctuation pattern, will be derived from the Triggerfish®, over a 24-hour period. Curves will be plotted for the IOP fluctuation.
Relationship between intraocular pulsation amplitude and BP 24-hours The relationship between intraocular pulsation amplitude and BP will be determined by the determination of the mean intraocular Triggerfish output (IOT), SIOT and DIOT and correlated to the mean BP, SBP and DBP.
Assess safety and tolerability 24-hours AEs and SAEs will be collected throughout the duration of the study
Trial Locations
- Locations (1)
Przemienienia Pańskiego Hospital, Poznan University of Medical Sciences Karol Marcinkowski
🇵🇱Poznan, Poland