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Comparison of Efficacy between Switching Intravitreal Ranibizumab and Aflibercept Injection in Non-responsive Neovascular Age-related Macular Degeneration Treated with Bevacizumab

Comparison of Efficacy between Switching Intravitreal Ranibizumab and Aflibercept Injection in Non-responsive Neovascular Age-related Macular Degeneration Treated with Bevacizumab

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20190928003
Enrollment
88
Registered
2019-09-28
Start date
2019-10-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non&#45

Interventions

responsive Neovascular Age&#45
related Macular Degeneration Treated with Bevacizumab participant will randomized into 2 groups as ranibizumab group and aflibercept group by compute&#45
generated block randomization &#45
Baseline data i.g. best corrected visual acuity&#44
central macular thickness collect from participants before switch to ranibizumab &#45
Paticipant treat by intravitral injection monthly &#45
Outcome data i.g. best corrected visual acuity&#44
central macular thickness&#44
color fundus photography collect after 3 months switching intravitral injection ,Non&#45
central macular thickness collect from participants before switch to aflibercept &#45
color fundus photography collect after 3 months switching intravitral injection
Active Comparator Drug,Active Comparator Drug
Non&#45

Sponsors

Department of ophthalmology, Phramongkutklao hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria Participant who was diagnosed as neovascular age-related macular degeneration and treated with intravitral Bevacizumab monthly at least 3 times and not responded to treatment which have one of these following conditions 1. Best corrected visual acuity not better than 5 letters or worst than baseline visual acuity 2.Macular edema or central macular thinkness decress less than 10 percent from baseline central macular thickness 3.New macular hemorrhage

Exclusion criteria

Exclusion criteria: Exclusion criteria 1.Patient who was treated with intravitral Ranibizumab or Aflibercept 2.Patient who was treated laser at macular 3.Patient who have other retinal diseases which cause macular edema e.g. Macular edema after surgery, diabetic macular edema 4.Eye diseases which interrupted research evaluation or affect to vision or have to treated with other medicines/ undergo surgery e.g. Worsen cataract, glaucoma, central retinal vein/artery occlusion

Design outcomes

Primary

MeasureTime frame
Best corrected visual acuit 3 months Early Treatment Diabetic Retinopathy Study (ETDRS) Chart

Secondary

MeasureTime frame
central macular thickness 3 months Optical Coherence Tomography : OCT

Countries

Thailand

Contacts

Public ContactFlt.Lt.Arissara Warichtrakul

Department of ophthalmology,Phramongkutklao hospital

evearisara@hotmail.com085-061-5432

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026