Skip to content

Intravitreal Avastin in Proliferative Retinopathies

Intravitreal Injections With Avastin in Proliferative Retinopathies Related to the Production of VEGF Having Different Causes

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00564148
Acronym
SITE-App
Enrollment
100
Registered
2007-11-27
Start date
2007-07-31
Completion date
2009-12-31
Last updated
2011-07-22

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

Conditions

Retinal Neovascularization

Keywords

antiVEGF therapy

Brief summary

The study intends to assess the effect of Avastin injections in different proliferative retinopathies due to different causes

Detailed description

Proliferative retinopathies due to different causes represent important causes for the visual acuity loss. Conventional treatments may sometimes improve the visual function, whereas other times, the visual acuity continue to decrease, in spite of all the medical, surgical or laser treatments. Intravitreal injections with anti-VEGF agents (ex. Avastin for our trial) seem to be an important tool for certain difficult situations in which at the ocular fundus, out of different reasons (advanced age, diabetes mellitus, retinal veins occlusions, etc)new pathologic vessels appear, causing devastating changes in the posterior and anterior segment as well.

Interventions

DRUGAvastin

2,5 mg Avastin intravitreal injections every 4 weeks, 6 months consecutively

Sponsors

Ophthalmological Association Edelweiss
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* clinical diagnosis of a proliferative retinopathy (AGE RELATED MACULAR DEGENERATION,DIABETIC PROLIFERATIVE RETINOPATHY, etc) * distance acuity \< 0.5 * age \> 20 years

Exclusion criteria

* noncooperative patients * ocular infections / inflammations

Design outcomes

Primary

MeasureTime frame
The following parameters will be assessed in order to evaluate the Avastin effect: visual acuity, lesions's area at the ocular fundusone year

Secondary

MeasureTime frame
The intraocular pressure will be measured during the whole study in order to assess the possible side effects of Avastin injectionsone year

Countries

Romania

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026