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Cataract DME - Peri vs. Intraop

Primary Purpose

Diabetic Macular Edema, Cataract

Status
Withdrawn
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Aflibercept injected Pre- and Post-operatively
Aflibercept injected intraoperatively
Sponsored by
Emory University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Diabetic Macular Edema focused on measuring anti-VEGF injections, pre-existing DME, cataract surgery

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults over age 18 with diabetes mellitus, diabetic macular edema and visually significant cataracts planning to undergo cataract surgery

Exclusion Criteria:

  • Patients who have undergone panretinal photocoagulation (PRP) in prior 4 months or an ocular condition (other than cataract and DME) that might affect visual acuity during course of study.
  • Patients with history of vitrectomy.
  • Patients with neovascular glaucoma.

Sites / Locations

  • Emory Clinic
  • Grady Health System

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Aflibercept injected Pre- and Post-operatively

Aflibercept injected intraoperatively

Arm Description

Pre- and Post-operative time of Aflibercept injections

Intraoperative time of Aflibercept injection

Outcomes

Primary Outcome Measures

Change in best-corrected visual acuity (BCVA)
BCVA is a measurement of the best vision correction that can be achieved, such as glasses, as measured on the standard Snellen eye chart. For example, if uncorrected eyesight is 20/200, but patient can see 20/20 with glasses, the BCVA is 20/20.

Secondary Outcome Measures

Change in optical coherence tomography (OCT) central subfield (CSF) thickness
Optical coherence tomography (OCT) is an important imaging modality in the evaluation and management of retinal diseases. Change in central subfield (CSF) thickness will be measured and recorded.
Total number of postoperative injections
Total number of postoperative injections will be calculated

Full Information

First Posted
April 17, 2019
Last Updated
December 23, 2020
Sponsor
Emory University
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1. Study Identification

Unique Protocol Identification Number
NCT03920878
Brief Title
Cataract DME - Peri vs. Intraop
Official Title
Peri- Versus Intra-operative Anti-vascular Endothelial Growth Factor Intravitreous Injections for Diabetic Macular Edema in Patients Undergoing Cataract Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Withdrawn
Why Stopped
The study team was unable to secure sufficient funding and administrative support.
Study Start Date
May 2020 (Anticipated)
Primary Completion Date
June 2020 (Anticipated)
Study Completion Date
June 2020 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Emory University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Goals of the study are to evaluate how peri-operative versus intra-operative anti-VEGF intravitreous injections affect visual acuity (BCVA) in patients with persistent diabetic macular edema who are undergoing cataract surgery; and to evaluate how peri-operative versus intra-operative anti-VEGF intravitreous injections affect OCT CSF thickness and total number of postoperative injections in patients with diabetic macular edema who are undergoing cataract surgery.
Detailed Description
Along with age, diabetes is a major risk factor for cataract formation, which can lead to significant vision loss and disability without medical intervention. Unfortunately, diabetic patients, particularly those with diabetic macular edema (DME), experience poorer visual outcomes after undergoing cataract surgery compared to non-diabetics. Reasons for this is multifactorial but includes an increased risk in the development of post-operative cystoid macular edema, and exacerbation of baseline DME. This poses a significant challenge in managing concomitant DME and visually-significant cataracts. Goals of the study are to evaluate how peri-operative versus intra-operative anti-VEGF intravitreous injections affect visual acuity (BCVA) in patients with persistent diabetic macular edema who are undergoing cataract surgery; and to evaluate how peri-operative versus intra-operative anti-VEGF intravitreous injections affect OCT CSF thickness and total number of postoperative injections in patients with diabetic macular edema who are undergoing cataract surgery.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Diabetic Macular Edema, Cataract
Keywords
anti-VEGF injections, pre-existing DME, cataract surgery

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
0 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Aflibercept injected Pre- and Post-operatively
Arm Type
Experimental
Arm Description
Pre- and Post-operative time of Aflibercept injections
Arm Title
Aflibercept injected intraoperatively
Arm Type
Active Comparator
Arm Description
Intraoperative time of Aflibercept injection
Intervention Type
Drug
Intervention Name(s)
Aflibercept injected Pre- and Post-operatively
Other Intervention Name(s)
EYELEA
Intervention Description
Three injections of aflibercept before cataract surgery, and aflibercept injections after surgery within 14-21 days of the day of surgery (number of injections depends on clinical exam findings, visual acuity and retinal thickness).
Intervention Type
Drug
Intervention Name(s)
Aflibercept injected intraoperatively
Other Intervention Name(s)
EYELEA
Intervention Description
Three injections of aflibercept before surgery and one injection of aflibercept during the course of the surgery by cataract surgeon.
Primary Outcome Measure Information:
Title
Change in best-corrected visual acuity (BCVA)
Description
BCVA is a measurement of the best vision correction that can be achieved, such as glasses, as measured on the standard Snellen eye chart. For example, if uncorrected eyesight is 20/200, but patient can see 20/20 with glasses, the BCVA is 20/20.
Time Frame
1 month, 3 months and 6 months after cataract surgery
Secondary Outcome Measure Information:
Title
Change in optical coherence tomography (OCT) central subfield (CSF) thickness
Description
Optical coherence tomography (OCT) is an important imaging modality in the evaluation and management of retinal diseases. Change in central subfield (CSF) thickness will be measured and recorded.
Time Frame
24 hours post-operatively, 1 month, 3 months and 6 months after cataract surgery
Title
Total number of postoperative injections
Description
Total number of postoperative injections will be calculated
Time Frame
6 months after cataract surgery

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults over age 18 with diabetes mellitus, diabetic macular edema and visually significant cataracts planning to undergo cataract surgery Exclusion Criteria: Patients who have undergone panretinal photocoagulation (PRP) in prior 4 months or an ocular condition (other than cataract and DME) that might affect visual acuity during course of study. Patients with history of vitrectomy. Patients with neovascular glaucoma.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew Hendrick, MD
Organizational Affiliation
Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Emory Clinic
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States
Facility Name
Grady Health System
City
Atlanta
State/Province
Georgia
ZIP/Postal Code
30322
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
No individual de-identified participant data (including data dictionaries) will be shared. Only composite results with publication will be shared.

Learn more about this trial

Cataract DME - Peri vs. Intraop

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