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Site of intravitreal injection and pain assessments from a randomized clinical trial

Site of intravitreal injection and pain assessments from a randomized clinical trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
TCTR
Registry ID
TCTR20201121001
Enrollment
80
Registered
2020-11-21
Start date
2020-11-23
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

Site of intravitreal injection and pain score Site of intravitreal injection pain

Interventions

Superonasal quadrant intrvitreal bevcizumab injection,Superotemporal quadrant intrvitreal bevcizumab injection,Inferonasal quadrant intrvitreal bevcizumab injection,Inferotemporal quadrant intrvitreal
Superonasal quadrant injection,Superotemporal quadrant injection,Inferonasal quadrant injection,Inferotemporal quadrant injection

Sponsors

Ratchadapiseksompotch Fund, Faculty of Medicine, Chulalongkorn University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to No maximum

Inclusion criteria

Inclusion criteria: Age > or = 20 years Diagnosed with neovascular (wet-type) age-related macular degeneration or diabetic macular edema or central retinal vein occlusion Confirmed with optical coherence tomography (OCT) or fundus fluorescein angiography (FFA) or both Need for intravitreal bevacizumab injection as the treatment for the first time in out-patient department or retina clinic, Department of Ophthalmology, KCMH

Exclusion criteria

Exclusion criteria: Patient with any of the following conditions: History of intravitreal injection Contraindicated in intravitreal injection Abnormality or scar on sclera, episclera or conjunctiva Ophthalmic disease requiring ophthalmic drop other than lubrication Intraocular pressure > or = 22 mmHg History of scleritis or episcleritis History of cranial nerve V abnormality History of intraocular surgery History of neovascular glaucoma Limitation of extraocular muscle interfering the injection

Design outcomes

Primary

MeasureTime frame
pain score at the end of intervention visual analog scale

Secondary

MeasureTime frame
Safety; Adverse events 0, 2, 4, 8, 12, 24, 36, 48 hrs Safety monitoring, vital sign,Safety; Adverse events check-out each period (48 hrs) PT, aPTT

Contacts

Public ContactChuthamas Ongprakobkul

Faculty of Medicine, Chulalongkorn University

chuthamas.tune@gmail.com+66958145928

Outcome results

None listed

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