General objective To evaluate the effect of regular tropical fruits intake on
intra-ocular pressure (IOP) and retinal nerve fibre layer thickness (RNFL) in primary
glaucoma patients.
Research hypothesis
There is a significant different in the IOP measurement between those whose taking
regular tropical fruits and not taking them at baseline, 1 month, 3 month and 6
month among patients with primary glaucoma.
There is a significant different in RNFL thickness between those whose taking
regular tropical fruits and not taking them at baseline, 1 month, 3 month and 6
month among patients with primary glaucoma.
Inclusion Criteria
Patient with confirmed diagnosis of POAG and PACG
Patient on medical treatment and achieved target IOP in last 6 months
Good compliance with pressure lowering agents
Exclusion Criteria
Poorly controlled diabetes mellitus, hypertension and hyperlipidaemia
Active smoker
Mentally challenge based on diagnosis
History of previous intraocular surgery other than uncomplicated cataract surgery
within past 6 months
Poor signal strength OCT RNFL
Patient with media opacities that affect the reliability of OCT measurements , such
as Cornea opacity, dense cataract with LOCS III of more than grade 2, vitreous
haemorrhage
Other optic neuropathy apart from glaucoma
History of taking antioxidant supplement 3 months prior to recruitment.
Methods of Data Collection
This study will be conducted after obtaining ethical approval from the Universiti Sains
Malaysia Ethical Committee (JPeM) and will be conducted in accordance to World Medical
Association Declaration of Helsinki ethical principles for medical research involving
human subjects.
Recruitment of Subject
Patient diagnosed with POAG and PACG attending Ophthalmology clinic, Hospital USM during
study duration and fulfilled study inclusion and exclusion criteria. An informed and
written consent will be taken and information form given to patients. The selected
patients will be randomized into 2 groups (A and B) using sequentially numbered, opaque
sealed envelopes (SNOSE). Group A patient will be consuming the chosen fruits and group B
patient will not consume them.
Interventional Protocol
Patients in Group A will have to consume 2 types of fresh fruits per week as 2 servings
once per day, daily for a 6-month duration. The chosen fruits are papaya, banana, mango
and orange, and 2 types of fruits per week will be determined by the primary
investigator. Size of the servings is according to the Malaysian Dietary Guideline 2020.
They must eat them raw, and not to process or cook them in any other way. The fruits will
be distributed by research assistant weekly throughout the study period. Patient will be
reminded weekly using text messages or phone call by a research assistant for the fruit's
consumption. Patients in group A and group B will be given a dietary diary throughout the
study period, where the patient will mark the intake of fruits listed. The purpose of the
diary is also to monitor patient intake of the fruits and daily diet as well.
IOP measurement
IOP measurement will be done using Goldmann Applanation Tonometer (GAT) in sitting
position by the primary investigator (Nurul Munirah) who will be blinded. GAT will be
calibrated daily before use to measure the IOP. Measurement of IOP will be done only at
8am - 10am (to prevent diurnal variation). Before IOP measurement, subjects are advised
to avoid drinking coffee or any caffeinated drink 24 hours before and only to take light
meal 2 hours before (to reduce the effect of hyperglycaemia and hydration on IOP). Only
one eye will be measured, if both eyes are eligible, only right eye will be selected
regardless of severity of glaucoma. Three readings of IOP will be measured and the mean
reading will be taken as result. IOP measurement will be taken at baseline, first, third
and sixth month post recruitment for group A and B.
OCT evaluation on RNFL thickness
Spectral domain Cirrus HD-OCT will be used to measure RNFL thickness and ONH parameters
by a trained personnel who is blinded. Patient's eye will be dilated and patient will sit
and rest his/her head on a support to keep it motionless in front of the OCT machine. The
OCT will then scan patient's eye without touching it. Scans with signal strength less
than 6, eye movement or blinking artifacts within the 1.73-mm radius around the ONH, or
with segmentation errors will be repeated. If there is unsatisfactory measurement after 3
attempts, the patient will be excluded from the study. OCT will be conducted at baseline,
first, third and sixth month post recruitment for group A and B.
Data Entry and Statistical Analysis
The data entry and analysis will be performed by using Statistical Package for the Social
Sciences (SPSS) version 29 licensed to USM.
Plans for minimizing study errors
These steps will be taken to minimize the errors while conducting the study:
The same instruments and equipment will be used for repeated measurement in this
study.
The measurement of IOP will be done at the same time (8am-10am) in a day for all
patients (to prevent diurnal variation).
OCT measurements will be performed by qualified and trained personnel only.