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Eylea and Lucentis for Macular Edema in Branch Retinal Vein Occlusion

Primary Purpose

Branch Retinal Vein Occlusion With Macular Edema

Status
Unknown status
Phase
Phase 4
Locations
Sweden
Study Type
Interventional
Intervention
Aflibercept Injection [Eylea]
Ranibizumab Injection [Lucentis]
Sponsored by
St. Erik Eye Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Branch Retinal Vein Occlusion With Macular Edema

Eligibility Criteria

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

Inclusion Criteria:

  • BRVO naïve patients, disease duration 1-6 months, BCVA 23-73 ETDRS letters (20/40-20/320), macula edema with intraretinal cysts and CRT > 300 micrometers (Cirrus)

Exclusion Criteria:

  • BRVO with neovascular component, intraocular surgery during the previous 3 months, earlier vitreoretinal surgery, vascular retinopathy of other cause, intraocular infection/inflammation, myocardial infarction och cerebrovascular stroke during the last 3 months.

Sites / Locations

  • St Eriks Eye HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Aflibercept

Ranibizumab

Arm Description

Aflibercept is given monthly (at least 3 times) until resolution of macular edema after which the patient is observed monthly. If there is recurrence of macula edema, the patient is given aflibercept according to a treat-and-extend regimen.

Ranibizumab is given monthly (at least 3 times) until resolution of macular edema after which the patient is observed monthly. If there is recurrence of macula edema, the patient is given ranibizumab according to a treat-and-extend regimen.

Outcomes

Primary Outcome Measures

Difference in time to recurrence of macular edema
Time, in weeks, from completion of loading dose to first recurrence of macular edema.

Secondary Outcome Measures

Comparison of the number of patients without ME in each treatment arm at one month after the first injection
The number of patients without macular edema at one month after the 1st injection in each treatment arm are compared
Comparison of the number of injections needed in each treatment arm to resolve ME
The number of injections needed for macular edema to resolve in each treatment arm are compared
Occurrence and evolution of macular ischemia over time
Area of non perfusion measured by OCT-angiography
Correlation between choroidal thickness and recurrence of ME and with non response to the treatment drugs.
Correlation of vision related QoL in patients with a good visual acuity and findings on visual fields, retinal sensitivity, macular ischemia and near VA.

Full Information

First Posted
October 15, 2018
Last Updated
December 2, 2020
Sponsor
St. Erik Eye Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03709745
Brief Title
Eylea and Lucentis for Macular Edema in Branch Retinal Vein Occlusion
Official Title
A Randomized Trial Comparing Treatment With Aflibercept and Ranibizuamab for Macular Edema After Branch Retinal Vein Occlusion
Study Type
Interventional

2. Study Status

Record Verification Date
December 2020
Overall Recruitment Status
Unknown status
Study Start Date
October 18, 2018 (Actual)
Primary Completion Date
November 2021 (Anticipated)
Study Completion Date
August 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
St. Erik Eye Hospital

4. Oversight

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

5. Study Description

Brief Summary
Comparing time to recurrence of macular edema after an initial loading dose of at least three monthly anti VEGF injections (aflibercept or ranibizumab) for macular edema in BRVO.
Detailed Description
One hundred and ten patients with macular edema (ME) secondary to BRVO are randomized (1:1) to treatment with intravitreal injections of aflibercept or ranibizumab. An initial loading dose of at least three monthly injections is given in the study eye until the ME is resolved. Then patients are observed at regular intervals, initially every four weeks until study completion. Total follow-up time is nine months from baseline to completion. If ME recurs, patients are treated according to a treat-and-extend algorithm. At every visit, visual acuity (VA) is measured with an ETDRS chart at 4 m. The fundus is examined by indirect ophthalmoscopy and by optical coherence tomography (OCT). Macular ischemia is evaluated with OCT angiography (OCT-A), visual field status with computerised perimetry and retinal sensitivity with microperimetry. Choroidal thickness is evaluated with enhanced depth imaging (EDI) OCT. Vision related quality of life (QoL) with NEI VFQ25.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Branch Retinal Vein Occlusion With Macular Edema

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
110 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Aflibercept
Arm Type
Active Comparator
Arm Description
Aflibercept is given monthly (at least 3 times) until resolution of macular edema after which the patient is observed monthly. If there is recurrence of macula edema, the patient is given aflibercept according to a treat-and-extend regimen.
Arm Title
Ranibizumab
Arm Type
Active Comparator
Arm Description
Ranibizumab is given monthly (at least 3 times) until resolution of macular edema after which the patient is observed monthly. If there is recurrence of macula edema, the patient is given ranibizumab according to a treat-and-extend regimen.
Intervention Type
Drug
Intervention Name(s)
Aflibercept Injection [Eylea]
Other Intervention Name(s)
Eylea
Intervention Description
Intravitreal injection is given as described in the arm description
Intervention Type
Drug
Intervention Name(s)
Ranibizumab Injection [Lucentis]
Other Intervention Name(s)
Lucentis
Intervention Description
Intravitreal injection is given as described in the arm description
Primary Outcome Measure Information:
Title
Difference in time to recurrence of macular edema
Description
Time, in weeks, from completion of loading dose to first recurrence of macular edema.
Time Frame
9 months
Secondary Outcome Measure Information:
Title
Comparison of the number of patients without ME in each treatment arm at one month after the first injection
Description
The number of patients without macular edema at one month after the 1st injection in each treatment arm are compared
Time Frame
1 month
Title
Comparison of the number of injections needed in each treatment arm to resolve ME
Description
The number of injections needed for macular edema to resolve in each treatment arm are compared
Time Frame
9 months
Title
Occurrence and evolution of macular ischemia over time
Description
Area of non perfusion measured by OCT-angiography
Time Frame
9 moths
Title
Correlation between choroidal thickness and recurrence of ME and with non response to the treatment drugs.
Time Frame
9 months
Title
Correlation of vision related QoL in patients with a good visual acuity and findings on visual fields, retinal sensitivity, macular ischemia and near VA.
Time Frame
9 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: BRVO naïve patients, disease duration 1-6 months, BCVA 23-73 ETDRS letters (20/40-20/320), macula edema with intraretinal cysts and CRT > 300 micrometers (Cirrus) Exclusion Criteria: BRVO with neovascular component, intraocular surgery during the previous 3 months, earlier vitreoretinal surgery, vascular retinopathy of other cause, intraocular infection/inflammation, myocardial infarction och cerebrovascular stroke during the last 3 months.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
David Epstein, MD PhD
Phone
+4686723000
Email
david.epstein@sll.se
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anders Kvanta, MD PhD
Organizational Affiliation
St. Erik Eye Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
St Eriks Eye Hospital
City
Stockholm
ZIP/Postal Code
11282
Country
Sweden
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
David Epstein, M.D
Phone
+46 86723228
Email
david.epstein@sankterik.se
First Name & Middle Initial & Last Name & Degree
Anders Kvanta, M.D PhD
Phone
+46 86720000
Email
anders.kvanta@sankterik.se
First Name & Middle Initial & Last Name & Degree
David Epstein, MD

12. IPD Sharing Statement

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Eylea and Lucentis for Macular Edema in Branch Retinal Vein Occlusion

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