The aim of the study is to measure RT (central, peripapillary and peripheral) in normal subjects and study the posibillity to reduce the variabillity of this measurements by normalisation. Futhermore, correlation of RT with axial lenght, gender and…
ID
Source
Brief title
Condition
- Retina, choroid and vitreous haemorrhages and vascular disorders
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Retinal Thickness and Retinal Nerve Fiber Layer thickness, measured by OCT
Normalised measurements (proprtional measurements)
Secondary outcome
age
gender
lenght
weight
refraction
Background summary
Optical Coherence Tomography (OCT) is a very sensative method to measure
retinal thickness (RT) and retinal nerve fiber layer-thickness (RNFL). OCT is a
save, non-invasive and non-contact procedure.
The latest generation OCT-scanners, the Startus OCT; Carl Zeiss Meditec Inc,
measures with an axial resolution of 10 micron. The Stratus software package
includes serveral scan aquisition- and analysis protocols, futhermore it
contains a normative database. Within the normative database there's a large
range of retinal thickness measurements; foveal RT 212 ± 20 micron, central
foveal RT 182 ± 23 micron. Several studies correlated RT in normal subjecs to
axial lenght, age, gender and Body Mass Index (BMI) without consensus of
opinion.
Our research group found a normal RT range of 207 ± 20 *m for foveal thickness
and 162 ± 22 *m for central foveal thickness, wich differs from the normative
database.
Due to this large range in normal RT, more subtle deviations will not be
registered as out of the ordinary. To reduce this variability one can calculate
propotions, by correlate the RT measurement to an non-pathologic area and
probably achieve normalisation of RT measurements.
Study objective
The aim of the study is to measure RT (central, peripapillary and peripheral)
in normal subjects and study the posibillity to reduce the variabillity of this
measurements by normalisation. Futhermore, correlation of RT with axial lenght,
gender and BMI will be studied.
Study design
a Study type: Inventory Observational
b Study design
To recrute healthy subjects, partners and/or companions of patients in our
outpatient clinic were approached.
Examination:
-full opthalmic examination
-capillairy blood level of glucose testing by finger prick (exclusion Diabetes
Mellitus)
-blood pressure measurement
-OCT-scans
c. amount of subjects: 60, of different age
d. study lenght, 6 months:
1 3 months for inclusion
2 data-management
e. Study department:
Academic Medical Center,Department of Ophthalmology,
dr. F.D. Verbraak, drs. P.H.B. Kok
mw. drs. P.H.B. Kok
Study burden and risks
The OCT-scanner is a safe non-invasive, non-contact procedure.
Meibergdreef 9
1105 AZ Amsterdam
Nederland
Meibergdreef 9
1105 AZ Amsterdam
Nederland
Listed location countries
Age
Inclusion criteria
No condtions in the eye or in general wich can influence the retinal thickness measurements
Exclusion criteria
Media opacities or other ocular disease on influence on RT measurement
Diabetes Mellitus
Glaucoma
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
CCMO | NL14695.018.06 |