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CompletedNCT00451763Updated Jul 23, 2008

Intravitreal Bevacizumab for Idiopathic Macular Telangiectasia

A Phase 3 interventional study of Intravitreal Injection of Bevacizumab (1.25 mg/0.05ml) in Retina and Telangiectasis, sponsored by University of Sao Paulo. Completed at 1 site in Brazil. Open to participants aged 40 Years and older. Per ClinicalTrials.gov, last updated 2008-07-23.

Sponsored by University of Sao Paulo · Phase 3, Interventional, and Treatment

Phase
Phase 3
Study type
Interventional
Enrollment
31
Allocation
Non-randomized
Ages
40 Years and older
Sex
All
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Study summary

Idiopathic Macular Telangiectasia is characterized by incompetent and dilated retinal capillaries in the foveolar region of unknown cause for retinal telangiectasia.

In Idiopathic Macular Telangiectasia, proliferative changes occur in the deep retinal capillary network, leading to intraretinal neovascularization that, unlike in age-related macular degeneration, seems to be retinal rather than choroidal in origin. Before the hemorrhagic and fibrotic state, these vessels may lead to exudation and decrease in the visual acuity. Long-term visual prognosis in patients with this complication may be poor and treatment with laser photocoagulation is unproven. Although newly reported treatment, by photodynamic therapy for neovascular membrane associated with Idiopathic Macular Telangiectasia, may show vision and angiographic stability in a few cases, the improvement may be transient. VEGF has been implicated as the major angiogenic stimulus responsible for neovascularization in AMD, ensuing specific anti-VEGF treatment in these cases.

The purpose of the study is to evaluate intravitreal injection of bevacizumab (1.25mg/0.05ml) in the treatment of Idiopathic Macular Telangiectasia.

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Conditions studied

  • Retina
  • Telangiectasis

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Keywords

  • Fovea centralis/pathology
  • Fundus oculi
  • Retinal neovascularization
  • Telangiectasis/diagnosis
  • Tomography, optical coherence
  • Vitreous Body/drug effects
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In context

Telangiectasis

153 studies on the registry are indexed under Telangiectasis; 16 are open to participants now.

This study's enrollment of 31 is close to the median of 30 across 107 interventional studies indexed under Telangiectasis.

Browse Telangiectasis studies →

Lead sponsor

University of Sao Paulo is the lead sponsor of 1,005 studies on the registry; 90 are open to participants now.

Of its 7 completed or terminated interventional studies of FDA-regulated products, 0 (0%) have results posted.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
40 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • patients with idiopathic macular telangiectasia
  • patient consent

Exclusion criteria

Exclusion Criteria:

  • heart attack or cerebrovascular attack
  • previous treatment for others retinopathy
  • media opacities that preclude visualization of the fundus
  • inability to understands the implications of the protocol
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Study design

Phase
Phase 3
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Single group
Masking
None (open label)
Enrollment
31 participants (actual)

Interventions

  • DrugIntravitreal Injection of Bevacizumab (1.25 mg/0.05ml)
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What researchers measure

Primary outcomes

  1. Visual acuity

  2. Optical coherence tomography

  3. Fluorescein angiography

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Study locations

1 site
  • From the Retina and Vitreous Service, Department of Ophthalmology. Sao Rafael Hospital, Monte Tabor Foudation
    Salvador, Bahia 41253-190, Brazil
08

References and documents

Publications

  • Maia OO Jr, Bonanomi MT, Takahashi WY, Nascimento VP, Takahashi BS. Intravitreal bevacizumab for foveal detachment in idiopathic perifoveal telangiectasia. Am J Ophthalmol. 2007 Aug;144(2):296-9. doi: 10.1016/j.ajo.2007.03.059. PubMed 17659962 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jul 23, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00451763
Lead sponsor
University of Sao Paulo
Collaborators
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior.
First posted
Mar 23, 2007
Start date
Jan 2006
Primary completion
Dec 2006
Completion
Dec 2007
Last update
Jul 23, 2008

Study contacts

Walter Y Takahashi, M.D.
study director · University of Sao Paulo
Otacilio O Maia Jr, M.D.
principal investigator · Sao Rafael Hospital, Monte Tabor Foudation

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2007. You cannot join it, but the record below documents what was studied.

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