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Short-term Additive Effect of Topical Ketorolac on the Management of Diabetic Macular Edema With Intravitreal Bevacizumab

Primary Purpose

DME

Status
Completed
Phase
Phase 2
Locations
Iran, Islamic Republic of
Study Type
Interventional
Intervention
prescription topical ketorolac in group 1
prescription artificial tear in group 2
prescription topical ketorolac in group 2
prescription artificial tear in group1
Sponsored by
Shahid Beheshti University of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for DME

Eligibility Criteria

30 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • BCVA≤20/40 and BCVA 20/400 and better
  • History of at least 1 intra-viteral bevacizumab (IVB) in the last 2 months
  • Requires 2 IVB in the next 12 weeks
  • Macular thickness >300 μm
  • NO Other eye diseases
  • Media clarity , pupillary dilation, and subject cooperation sufficient for adequate fundus photographs

Exclusion Criteria:

  • hgb A1c> 8
  • high risk PDR
  • Macular edema due to a cause other than diabetic retinopathy
  • Any other ocular condition that visual acuity would not improve from resolution of edema (eg.foveal atrophy)
  • Prior treatment with intravitreal or peribulbar corticosteroid injection during last 3months
  • History of macular photocoagulation during the last 6 months
  • intraocular surgery(except cataract surgery)
  • Cataract extractionin less than 6 months ago
  • Uveitis ,NVG ,exudative AMD, HR PDR.
  • Uncontrolled glaucoma
  • Vitreomacular traction or epiretinal membrane

Sites / Locations

  • Ophthalmic Research Center

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Active Comparator

Active Comparator

Active Comparator

Arm Label

usage of topical ketorolac in group1

usage of artificial tear in group 2

usage of artificial tear in group 1

usage of topical ketorolac in group2

Arm Description

usage of topical ketorolac every 6 hour in the first interval and then artificial tear every 6 hour as a placebo in the second interval.

usage of artificial tear every 6 hour in the first interval and then topical ketorolac every 6 hour as a placebo in the second interval.

usage of topical ketorolac every 6 hour in the first interval and then artificial tear every 6 hour as a placebo in the second interval

usage of artificial tear every 6 hour in the first interval and then topical ketorolac every 6 hour as a placebo in the second interval

Outcomes

Primary Outcome Measures

visual acuity
Snellen E-chart

Secondary Outcome Measures

Centeral macular thickness
Ophtical Cohearence Tomography

Full Information

First Posted
October 2, 2019
Last Updated
February 20, 2021
Sponsor
Shahid Beheshti University of Medical Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT04119921
Brief Title
Short-term Additive Effect of Topical Ketorolac on the Management of Diabetic Macular Edema With Intravitreal Bevacizumab
Official Title
Short-term Additive Effect of Topical Ketorolac on the Management of Diabetic Macular Edema With Intravitreal Bevacizumab
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
June 1, 2018 (Actual)
Study Completion Date
June 20, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shahid Beheshti University of Medical Sciences

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Purpose: To evaluate the short-term effect of adding topical ketorolac to the management of diabetic macular edema (DME) with intravitreal bevacizumab (IVB). Setting: Ophthalmology department of Imam Hossein and Torfe Medical Centers. Ophthalmic Epidemiology Research Center of Shahid Beheshti University of Medical Sciences Methods: In a randomized double-masked placebo-controlled crossover clinical trial, all eyes with DME with best-corrected visual acuity (BCVA) between 20/40 and 20/400 were included. They should have had at least one intravitreal anti-VEGF injection in the past 2 months. They were randomized into two groups. Both groups received two IVB injections with 6-week interval. One group received topical ketorolac every 6 hour in the first interval and then artificial tear every 6 hour as a placebo in the second interval. The other group received the opposite medications. Best-corrected visual acuity (BCVA) and central macular thickness (CMT) evaluations were repeated at the termination of each treatment period i.e. at 6 and 12 weeks. The main outcome measure was BCVA changes in logMAR and the second outcome was CMT changes. The interim analysis of this study is presented in this report.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
DME

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
usage of topical ketorolac in group1
Arm Type
Active Comparator
Arm Description
usage of topical ketorolac every 6 hour in the first interval and then artificial tear every 6 hour as a placebo in the second interval.
Arm Title
usage of artificial tear in group 2
Arm Type
Active Comparator
Arm Description
usage of artificial tear every 6 hour in the first interval and then topical ketorolac every 6 hour as a placebo in the second interval.
Arm Title
usage of artificial tear in group 1
Arm Type
Active Comparator
Arm Description
usage of topical ketorolac every 6 hour in the first interval and then artificial tear every 6 hour as a placebo in the second interval
Arm Title
usage of topical ketorolac in group2
Arm Type
Active Comparator
Arm Description
usage of artificial tear every 6 hour in the first interval and then topical ketorolac every 6 hour as a placebo in the second interval
Intervention Type
Drug
Intervention Name(s)
prescription topical ketorolac in group 1
Intervention Description
topical ketorolac every 6 hour in the first interval and then artificial tear every 6 hour as a placebo in the second interval.
Intervention Type
Drug
Intervention Name(s)
prescription artificial tear in group 2
Intervention Description
artificial tear every 6 hour in the first interval and then topical ketorolac every 6 hour as a placebo in the second interval.
Intervention Type
Drug
Intervention Name(s)
prescription topical ketorolac in group 2
Intervention Description
artificial tear every 6 hour in the first interval and then topical ketorolac every 6 hour as a placebo in the second interval.
Intervention Type
Drug
Intervention Name(s)
prescription artificial tear in group1
Intervention Description
topical ketorolac every 6 hour in the first interval and then artificial tear every 6 hour as a placebo in the second interval.
Primary Outcome Measure Information:
Title
visual acuity
Description
Snellen E-chart
Time Frame
6 weeks
Secondary Outcome Measure Information:
Title
Centeral macular thickness
Description
Ophtical Cohearence Tomography
Time Frame
6 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
30 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: BCVA≤20/40 and BCVA 20/400 and better History of at least 1 intra-viteral bevacizumab (IVB) in the last 2 months Requires 2 IVB in the next 12 weeks Macular thickness >300 μm NO Other eye diseases Media clarity , pupillary dilation, and subject cooperation sufficient for adequate fundus photographs Exclusion Criteria: hgb A1c> 8 high risk PDR Macular edema due to a cause other than diabetic retinopathy Any other ocular condition that visual acuity would not improve from resolution of edema (eg.foveal atrophy) Prior treatment with intravitreal or peribulbar corticosteroid injection during last 3months History of macular photocoagulation during the last 6 months intraocular surgery(except cataract surgery) Cataract extractionin less than 6 months ago Uveitis ,NVG ,exudative AMD, HR PDR. Uncontrolled glaucoma Vitreomacular traction or epiretinal membrane
Facility Information:
Facility Name
Ophthalmic Research Center
City
Tehran
Country
Iran, Islamic Republic of

12. IPD Sharing Statement

Learn more about this trial

Short-term Additive Effect of Topical Ketorolac on the Management of Diabetic Macular Edema With Intravitreal Bevacizumab

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