The Effect Of Tropical Fruits In Patients With Primary Glaucoma

March 5, 2024 updated by: NURUL MUNIRAH BINTI MOHAMAD, Hospital Universiti Sains Malaysia

A Randomized Controlled Trial Of The Effect Of Tropical Fruits On Intraocular Pressure And Retinal Nerve Fibre Layer Thickness In Patients With Primary Glaucoma

To evaluate the effect of regular tropical fruits intake in primary glaucoma patients.

Methodology :

Research Design Randomized controlled trial

Study Duration February 2024-June 2025

Study Location

1. Ophthalmology Clinic, Hospital Universiti Sains Malaysia, Kelantan

Source Reference Population Adults with primary glaucoma in Peninsular Malaysia

Study Source Population Adults with primary glaucoma attending Ophthalmology clinic, Hospital Universiti Sains Malaysia during study duration.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

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

  1. 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.
  2. 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

  1. Patient with confirmed diagnosis of POAG and PACG
  2. Patient on medical treatment and achieved target IOP in last 6 months
  3. Good compliance with pressure lowering agents

Exclusion Criteria

  1. Poorly controlled diabetes mellitus, hypertension and hyperlipidaemia
  2. Active smoker
  3. Mentally challenge based on diagnosis
  4. History of previous intraocular surgery other than uncomplicated cataract surgery within past 6 months
  5. Poor signal strength OCT RNFL
  6. 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
  7. Other optic neuropathy apart from glaucoma
  8. 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.

  • Paired T-test
  • Chi-square test
  • A one-way repeated measures analysis of variance (RM ANOVA)

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.

Study Type

Interventional

Enrollment (Estimated)

102

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

  • Name: Liza Sharmini Ahmad Tajudin, Prof. Dr.
  • Phone Number: +60199179227
  • Email: liza@usm.my

Study Locations

    • Kota Bharu
      • Kubang Kerian, Kota Bharu, Malaysia, 16150
        • Recruiting
        • Univerisiti Sains Malaysia
        • Contact:
        • Principal Investigator:
          • NURUL MUNIRAH MOHAMAD, MBBCh
        • Sub-Investigator:
          • PROF DR LIZA SHARMINI AHMAD TAJUDIN
        • Sub-Investigator:
          • ASS PROF DR ROHANA ABD JALIL

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  1. Patient with confirmed diagnosis of POAG and PACG
  2. Patient on medical treatment and achieved target IOP in last 6 months
  3. Good compliance with pressure lowering agents

Exclusion Criteria:

  1. Poorly controlled diabetes mellitus, hypertension and hyperlipidaemia
  2. Active smoker
  3. Mentally challenge based on diagnosis
  4. History of previous intraocular surgery other than uncomplicated cataract surgery within past 6 months
  5. Poor signal strength OCT RNFL
  6. 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
  7. Other optic neuropathy apart from glaucoma
  8. History of taking antioxidant supplement 3 months prior to recruitment

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Tropical Fruits
patient will be consuming the chosen fruits, according to the size of the serving following Malaysian Dietary Guideline 2020
papaya, mango, banana, orange
No Intervention: Normal diet
patient will consume normal diet as usual

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
intraocular pressure
Time Frame: baseline, at 1 month , at 3 months and 6 months
tonometer
baseline, at 1 month , at 3 months and 6 months
retinal nerve fibre layer
Time Frame: baseline, at 1 month , at 3 months and 6 months
Spectral domain Cirrus HD-OCT
baseline, at 1 month , at 3 months and 6 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Nurul Munirah Mohamad, Dr, Department of Ophthalmology School of Medical Sciences Universiti Sains Malaysia,Health Campus.
  • Study Chair: Liza Sharmini Ahmad Tajudin, Prof. Dr., Department of Ophthalmology School of Medical Sciences Universiti Sains Malaysia,Health Campus.
  • Study Director: Rohana Abd Jalil, Ass. Prof. Dr., Department of Ophthalmology School of Medical Sciences Universiti Sains Malaysia,Health Campus.
  • Study Director: Fatimah Suhaila Sukaimy, Dr, Department of Ophthalmology Hospital Tengku Ampuan Afzan, Ministry of Health, Malaysia

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

February 1, 2024

Primary Completion (Estimated)

July 1, 2024

Study Completion (Estimated)

July 1, 2025

Study Registration Dates

First Submitted

October 1, 2023

First Submitted That Met QC Criteria

October 1, 2023

First Posted (Actual)

October 6, 2023

Study Record Updates

Last Update Posted (Actual)

March 7, 2024

Last Update Submitted That Met QC Criteria

March 5, 2024

Last Verified

March 1, 2024

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • RSCH ID-23-03744-7U6

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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