Protocol summary
-
Study aim
-
To evaluate the effect of post-operative latanoprost administration on central macular thickness (CMT) after uncomplicated cataract surgery in glaucoma patients
-
Design
-
Two-arm parallel group randomized trial with blinded outcome assessment. Randomization was centralized and computerized with concealed randomization sequence carried out at an external site
-
Settings and conduct
-
The study was conducted at Farabi Eye Hospital (Tehran University of Medical Sciences, Tehran, Iran).
Patients without any risk factor or abnormality such as cystic changes in the macula in pre-op OCT were included for allocation. Patients were allocated into two groups; In the first group, on postoperative day 1, patients continued receiving latanoprost and other antiglaucoma topical agents to control the IOP. In the second group, on postoperative day 1, latanoprost was discontinued, and patients received any other antiglaucoma topical agents to control the IOP. All surgeries and post-operative examinations were done by the same expert cataract surgeon (GH. F.). Patients were aware of the allocation, while surgeon/examiner (GH. F.), outcome assessor/analyst (M.Y.) were masked to the patient allocation which was done by M.M.
-
Participants/Inclusion and exclusion criteria
-
Glaucoma patients treating with latanoprost; who need cataract surgery; and had no other risk factors for the development of pseudophakic macular edema; and with no abnormality in pre-operative optical coherence tomography (OCT) were included.
-
Intervention groups
-
Patients were allocated into two groups; continue latanoprost and discontinue latanoprost.
-
Main outcome variables
-
Main outcome was defined as central macular thickness (CMT) change from baseline measured by OCT imaging. Secondary outcomes were incidence of clinical cystoid macular edema, incidence of significant increase in CMT, visual acuity, IOP, and number of antiglaucoma medications.
General information
-
Reason for update
-
-
Acronym
-
-
IRCT registration information
-
IRCT registration number:
IRCT2016081329326N1
Registration date:
2016-09-11, 1395/06/21
Registration timing:
prospective
Last update:
2019-10-15, 1398/07/23
Update count:
3
-
Registration date
-
2016-09-11, 1395/06/21
-
Registrant information
-
-
Recruitment status
-
Recruitment complete
-
Funding source
-
Vice chancellor for research, Tehran University of Medical Sciences
-
Expected recruitment start date
-
2016-09-21, 1395/06/31
-
Expected recruitment end date
-
2018-09-21, 1397/06/30
-
Actual recruitment start date
-
2016-09-21, 1395/06/31
-
Actual recruitment end date
-
2018-09-03, 1397/06/12
-
Trial completion date
-
2018-09-03, 1397/06/12
-
Scientific title
-
Effect of continuation of prostaglandin analogue use on the incidence of Cystoid Macular Edema (CME) following uncomplicated cataract surgery in glaucoma patients
-
Public title
-
Effect of Latanaprost eye drop on retina after cataract surgery in glaucoma patients
-
Purpose
-
Prevention
-
Inclusion/Exclusion criteria
-
Inclusion criteria:
Glaucoma patients with 18 years old or more
Treating with topical latanoprost 0.005% eye drop at least for 6 months with or without other antiglaucoma topical agents
Who needed cataract surgery (phacoemulsification)
Exclusion criteria:
History of any intraocular surgery, intravitreal injections, or retinal laser
History of trauma
Non-glaucomatous optic neuropathy
High myopia
History of diabetic retinopathy, any age-related macular degeneration (AMD), uveitis, retinal detachment (RD), epiretinal membrane (ERM), and retinal vascular disorders
An occurrence of CME in the fellow eye following previous cataract surgery
Recent history of NSAID therapy (topical or oral)
Any abnormality in fundus examination except for glaucomatous changes
Any abnormality in pre-operative macular OCT.
-
Age
-
From 18 years old
-
Gender
-
Both
-
Phase
-
2
-
Groups that have been masked
-
- Care provider
- Outcome assessor
- Data analyser
-
Sample size
-
Target sample size:
166
Actual sample size reached:
156
-
Randomization (investigator's opinion)
-
Randomized
-
Randomization description
-
A computer-based program (Excel® Microsoft Office software version 2016) to assign our samples to the two groups was used. The randomization used was block permutated randomization with the random block size of 2,4 and 6. The random sequence obtained by a biostatistician and it was concealed from the research group by coloring the background of cells in Excel datasheet. Whenever each new patient was a candidate for allocation, one author (M.M) uncolored the devoted cell and allocated the patient according to the written number, 1 for continuing and 2 for stop continuing latanoprost.
-
Blinding (investigator's opinion)
-
Single blinded
-
Blinding description
-
The design of the RCT was single-masked. Patients were aware of the allocation, while surgeon/examiner (GH.F.), outcome assessor/analyst (M.Y.) were masked to the patient allocation which was done by M.M.
-
Placebo
-
Not used
-
Assignment
-
Parallel
-
Other design features
-
Ethics committees
1
-
Ethics committee
-
-
Approval date
-
2016-08-06, 1395/05/16
-
Ethics committee reference number
-
IR.TUMS.FARABIH.REC.1395.397
Health conditions studied
1
-
Description of health condition studied
-
Cystoid macular edema
-
ICD-10 code
-
H35.8
-
ICD-10 code description
-
Other specified retinal disorders
Primary outcomes
1
-
Description
-
Central Macular Thickness
-
Timepoint
-
Before intervention, 1 month after intervention and 3 months after intervention
-
Method of measurement
-
Using OCT-SD imaging
Secondary outcomes
1
-
Description
-
Intraocular pressure
-
Timepoint
-
Before intervention, 1 month after intervention and 3 months after intervention
-
Method of measurement
-
Goldmann tonometry
2
-
Description
-
Visual acuity
-
Timepoint
-
Before intervention, 1 month after intervention and 3 months after intervention
-
Method of measurement
-
Snellen chart
3
-
Description
-
Number of medications needed to control the IOP
-
Timepoint
-
Before intervention, 1 month after intervention and 3 months after intervention
-
Method of measurement
-
Medical records
4
-
Description
-
Incidence of clinical cystoid macular edema
-
Timepoint
-
Before intervention, 1 month after intervention and 3 months after intervention
-
Method of measurement
-
Clinical Fundus examination
5
-
Description
-
Incidence of significant increase in CMT
-
Timepoint
-
Before intervention, 1 month after intervention and 3 months after intervention
-
Method of measurement
-
Defined as ≥ 50 µm compared to the baseline in OCT imaging
Intervention groups
1
-
Description
-
Intervention group : In this group, prostaglandin analogue (Latanaprost eye drop) is discontinued immediately after cataract surgery for 3 months and replaced with other antiglaucoma agents to control IOP.
-
Category
-
Treatment - Drugs
2
-
Description
-
Control group: Prostaglandin analogue (Latanaprost eye drop, one drop before sleep at night) after cataract surgery will be continued.
-
Category
-
Treatment - Drugs
1
-
Sponsor
-
-
Grant name
-
-
-
Grant code / Reference number
-
-
-
Is the source of funding the same sponsor organization/entity?
-
Yes
-
Title of funding source
-
Tehran University of Medical Sciences
-
Proportion provided by this source
-
100
-
Public or private sector
-
Public
-
Domestic or foreign origin
-
Domestic
-
Category of foreign source of funding
-
empty
-
Country of origin
-
-
Type of organization providing the funding
-
Academic
Sharing plan
-
Deidentified Individual Participant Data Set (IPD)
-
No - There is not a plan to make this available
-
Justification/reason for indecision/not sharing IPD
-
Not published due to Farabi Eye Research department guidelines.
-
Study Protocol
-
Yes - There is a plan to make this available
-
Statistical Analysis Plan
-
No - There is not a plan to make this available
-
Informed Consent Form
-
Yes - There is a plan to make this available
-
Clinical Study Report
-
Yes - There is a plan to make this available
-
Analytic Code
-
No - There is not a plan to make this available
-
Data Dictionary
-
No - There is not a plan to make this available
-
Title and more details about the data/document
-
The study protocol and informed consent will be shared privately, but a report of the study will be shared in public. Depending on the request, all data may be shared.
-
When the data will become available and for how long
-
After completion of the study, for 12 months.
-
To whom data/document is available
-
Just for academic researchers.
-
Under which criteria data/document could be used
-
Just for scientific and research purposes.
-
From where data/document is obtainable
-
Please send an e-mail with relevant content to corresponding author:
m-mirghorbani@razi.tums.ac.ir
Seyed Masoud Mirghorbani
Resident of Ophthalmology
Farabi Eye Hospital, Qazvin sq, South Kargar st, Tehran
+982155400003
-
What processes are involved for a request to access data/document
-
Anyone who needs detailed information on study protocol and informed consent can e-mail to the corresponding author and request for the data.
The request will be evaluated in a few weeks.
-
Comments
-
Trial results
-
Please tick if results have been published
-
Yes
-
Summary result posting date
-
2019-10-15, 1398/07/23
-
Table of baseline comparison
-
-
Participant flow diagram
-
-
Table of variable outcomes' results
-
-
Table of adverse events
-
-
First publication date
-
2019-10-01, 1398/07/09
-
Abstract of published paper
-
Purpose
To evaluate the effect of postoperative latanoprost administration on central macular thickness (CMT) after uneventful cataract surgery in glaucoma patients.
Setting
Farabi Eye Hospital, Tehran, Iran.
Design
Prospective randomized clinical trial.
Methods
In this single-masked trial, glaucoma patients treated with latanoprost who had no other risk factor for the development of pseudophakic macular edema were randomly allocated to continuation of latanoprost or discontinuation of the drop after uneventful cataract surgery. At baseline and postoperatively at 1 month and 3 months, patients had complete ocular examinations and CMT measurements using optical coherence tomography. The main outcome measure was the change in the CMT between baseline measurements and postoperative measurements at 1 month and 3 months.
Results
One hundred fifty-six eyes (latanoprost 76; discontinuation 80) finished the trial. There were no differences in baseline patient demographics or characteristics, including the CMT, between the two groups. There was transient increase in the mean CMT by 12 μm ± 49 (SD) in the latanoprost group at 1 month (P = .03); however, the value returned to baseline by 3 months (6 ± 55 μm; P = .27). The between-group difference in the mean change in the CMT from baseline was −3.1 μm (95% confidence interval [CI], −18.4 to 12.0; P = .68) after 1 month and −10.5 μm (95% CI, −26.6 to 5.5; P = .19) after 3 months; the differences were not significant.
Conclusion
Latanoprost administration after cataract surgery had no measurable effect on macular thickness.