- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02582411
Laser Speckle Flowgraphy in Caucasians: Age Dependence and Comparison With Doppler Optical Coherence Tomography
Study Overview
Status
Conditions
Intervention / Treatment
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Vienna, Austria, 1090
- Department of Clinical Pharmacology, Medical University of Vienna
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Men and women aged over 18 years, nonsmokers
- Subject is generally healthy with no current significant or a history of a significant neurological, cardiovascular, pulmonary (including asthma), hepatic, metabolic, rheumatic, autoimmune, hematological or renal disorder, as determined by the investigator's clinical judgment through collection of medical history and performance of a physical examination. A significant disorder is defined as a disease or medical condition associated with impaired health status, requiring regular or current medical treatment and/or follow up. For the purposes of this study, an investigator may classify a medical condition as a nonsignificant disorder despite the fact that the subject receives treatment. Subjects having controlled Stage 1 hypertension (blood pressure of 140-159 mmHg systolic and/or 90- 99 mmHg diastolic) are eligible for participation in this study.
- Normal ophthalmic findings, ametropia < 6 Dpt
Exclusion Criteria:
- Symptoms of a clinically relevant illness in the 3 weeks before the first study day
- Wearing of contact lenses
- Ocular infection or clinically significant inflammation
- Ocular surgery in the 3 months preceding the study
- Blood donation in the 3 weeks preceding the study
- Pregnancy, planned pregnancy or lactating
- Opacities of the cornea (e.g. corneal scars, corneal oedema), the lens (e.g. Lens opacities classification system version II (LOCS-II) grading > 2, posterior capsule opacification) or the vitreous (e.g. vitreous haemorrhage, asteroid hyalosis)
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Group 1: 18-34 years
Patients in age group 18-34 years
|
A commercially available LSFG (Softcare, Fukutsu, Japan) system will be used in the present study.
The LSFG device consists of a fundus camera equipped with a diode laser with a wavelength if 830 nm and charge-coupled device.
NB, the relative velocity of blood flow, is derived from the pattern of speckle contrast produced by the interference of a laser scattered by blood cells moving in the ocular fundus.
Images are acquired continuously at the rate of 30 frames per seconds in a 4-second time period and stored on a personal computer.
Heartbeat map of the optic nerve head and the retina/choroid is generated
Other Names:
A dual-beam bidirectional Doppler OCT system comprises a broadband superluminescent diode (SLD) with a central wavelength of 840 (spectral bandwidth 54 nm) and two CCD cameras with a maximum readout rate of 20 kHz. The system provides a resolution (in tissue) of about 6 and 18 μm in axial and lateral direction, respectively. The sample, i.e. the retinal vessel under study, is illuminated by two probe beams separated by their polarization properties. Light back scattered and backreflected from the sample is spectrally detected by two identical spectrometers and postprocessing, i.e. calculation the phase shift due moving scatterers within the sample, is carried out by a personal computer with software written in National Instruments LabView. The power of both probe beams incident on the cornea is 650 μW, which is below the ANSI (American National Standard Institute) limits for small source ocular exposure to a laser beam within the measuring time. |
|
Group 2: 35-49 years
Patients in age group 35-49 years
|
A commercially available LSFG (Softcare, Fukutsu, Japan) system will be used in the present study.
The LSFG device consists of a fundus camera equipped with a diode laser with a wavelength if 830 nm and charge-coupled device.
NB, the relative velocity of blood flow, is derived from the pattern of speckle contrast produced by the interference of a laser scattered by blood cells moving in the ocular fundus.
Images are acquired continuously at the rate of 30 frames per seconds in a 4-second time period and stored on a personal computer.
Heartbeat map of the optic nerve head and the retina/choroid is generated
Other Names:
|
|
Group 3: 50-64 years
Patients in age group 50-64 years
|
A commercially available LSFG (Softcare, Fukutsu, Japan) system will be used in the present study.
The LSFG device consists of a fundus camera equipped with a diode laser with a wavelength if 830 nm and charge-coupled device.
NB, the relative velocity of blood flow, is derived from the pattern of speckle contrast produced by the interference of a laser scattered by blood cells moving in the ocular fundus.
Images are acquired continuously at the rate of 30 frames per seconds in a 4-second time period and stored on a personal computer.
Heartbeat map of the optic nerve head and the retina/choroid is generated
Other Names:
|
|
Group 4: 65-80 years
Patients in age group 65-80 years
|
A commercially available LSFG (Softcare, Fukutsu, Japan) system will be used in the present study.
The LSFG device consists of a fundus camera equipped with a diode laser with a wavelength if 830 nm and charge-coupled device.
NB, the relative velocity of blood flow, is derived from the pattern of speckle contrast produced by the interference of a laser scattered by blood cells moving in the ocular fundus.
Images are acquired continuously at the rate of 30 frames per seconds in a 4-second time period and stored on a personal computer.
Heartbeat map of the optic nerve head and the retina/choroid is generated
Other Names:
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Relative flow volume (LSFG)
Time Frame: 3 weeks
|
3 weeks
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Systemic blood pressure
Time Frame: 3 weeks
|
3 weeks
|
|
Intraocular pressure
Time Frame: 3 weeks
|
3 weeks
|
Collaborators and Investigators
Sponsor
Publications and helpful links
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- OPHT-040415
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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