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Monoclonal Antibodies
Intravitreal infliximab. for Diabetic Macular Edema
Phase 1 & 2
Waitlist Available
Led By Farzin Forooghian, MD
Research Sponsored by Icahn School of Medicine at Mount Sinai
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up one, two, and three months
Awards & highlights
Study Summary
The purpose of this study is to determine if intravitreal infliximab is a safe and effective treatment for macular edema secondary to diabetes.
Eligible Conditions
- Diabetic Macular Edema
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ three months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~three months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Best-corrected visual acuity
Secondary outcome measures
Macular thickness
Side effects data
From 2020 Phase 4 trial • 42 Patients • NCT0300639352%
Laceration
38%
Headache
24%
Bruises
19%
Sore throat
14%
Muscle tension
10%
Heartburn
10%
Fatigue
10%
Change in urination
10%
Nausea
10%
Dizziness
10%
Itchiness
5%
Pain in joints
5%
Menstruation
5%
Stomach ache
5%
Syncope
5%
Migraine
5%
Chest pain
5%
Swelling
5%
Bloody stool
5%
Pain in leg
5%
Allergies
5%
Change in blood pressure
5%
Vertigo
5%
Change in appetite
5%
Numbness
5%
Motor vehicle accident
100%
80%
60%
40%
20%
0%
Study treatment Arm
Infliximab
Placebo
Trial Design
1Treatment groups
Experimental Treatment
Group I: Intravitreal infliximab.Experimental Treatment1 Intervention
Find a Location
Who is running the clinical trial?
Icahn School of Medicine at Mount SinaiLead Sponsor
862 Previous Clinical Trials
525,498 Total Patients Enrolled
Farzin Forooghian, MDPrincipal InvestigatorIcahn School of Medicine at Mount Sinai
1 Previous Clinical Trials
10 Total Patients Enrolled
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
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