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Change of OCT findings after Intravitreal Anti-VEGF injection in patients with diabetic tractional retinal detachment : A Randomized Controlled Trial

Change of OCT findings after Intravitreal Anti-VEGF injection in patients with diabetic tractional retinal detachment : A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
TCTR
Registry ID
TCTR20210524001
Enrollment
80
Registered
2021-05-24
Start date
2021-06-01
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

Tractional retinal detachment in patient with proliferative diabetic retinopathy Tractional retinal detachment Anti VEGF diabetic retinopathy OCT

Interventions

Intravitreal anti-VEGF (Bevacizumab, Aflibercept, Ranibizumab) injection on day0, day 30, day 60,Patient will be follow up with OCT on day 0, 30, 60 and 90
Experimental Drug,No Intervention No treatment
Anti VEGF injection,Control

Sponsors

Research Funds, Faculty of medicine, KKU
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age > 18 years 2. With the following characteristics 2.1) underlying disease of type 1 or type 2 diabetes mellitus 2.2) diagnosed with PDR with TRD requiring surgery 2.3) OCT scans on the enroll day with good interpretable quality showing fibrous traction on preretinal area and tractional retinal detachment 2.4) If two eyes are elligible, only one eye per patient (the eye with worse visual acuity) will be included in the study.

Exclusion criteria

Exclusion criteria: 1. Patient with center-involved DME with macular edema from component other than traction 2. Patient with severe anterior segment pathology precluding OCT scans, fundus examination (i.e. dense cataract, dense vitreous hemorrhage) 3. Previous intraocular surgery (except uncomplicated cataract surgery) 4. Previous Injection into study eyes within 6 months 5. Patient contraindicated to intravitreal injection (i.e endophthalmitis) 6. Patient with other ocular pathology causing possible neovascularization, retinal detachment or fibrous traction in study eyes (Traumatic retinal detachment, Uveitis, Retinal vascular disease, Congenital vitreoretinopathy 7. Patient denied intravitreal injection

Design outcomes

Primary

MeasureTime frame
Change of tractional degree 1 month OCT

Secondary

MeasureTime frame
Change of detachment degree 1 month OCT

Countries

Thailand

Contacts

Public ContactKanpirom Tangpontirak

student

kanpta@kku.ac.th0830304399

Outcome results

None listed

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