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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01032109
Other study ID # PCBK610
Secondary ID
Status Completed
Phase N/A
First received December 12, 2009
Last updated February 25, 2016
Start date October 2006
Est. completion date May 2008

Study information

Verified date February 2016
Source Kumamoto University
Contact n/a
Is FDA regulated No
Health authority Japan: Institutional Review Board
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare 12-month results of two single initial treatments—photodynamic therapy with verteporfin alone and this therapy combined with intravitreal bevacizumab—for neovascular age-related macular degeneration, not including patients with polypoidal choroidal vasculopathy who were presumed to have age-related macular degeneration.


Recruitment information / eligibility

Status Completed
Enrollment 45
Est. completion date May 2008
Est. primary completion date May 2008
Accepts healthy volunteers No
Gender Both
Age group 50 Years and older
Eligibility Inclusion Criteria:

- choroidal neovascularization caused by age-related macula degeneration

- no previous treatment

- a follow-up at least 12 months

- a baseline visual acuity ranging from a letter score of 0 to 70 on the Early Treatment Diabetic Retinopathy Study chart

Exclusion Criteria:

- choroidal neovascularization caused by other eye diseases

- ocular surgery within the past 3 mouths

- history of uveitis

- intraocular pressure higher than 25 mmHg, or glaucoma

- history of systemic or ocular thromboembolic events.

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Drug:
Bevacizumab
A single intravitreal injection of 1.25 mg of bevacizumab (0.05 mL of solution prepared from Avastin, 100 mg/4 mL vial) was performed within 2 weeks after PDT treatment.

Locations

Country Name City State
Japan Department of Ophthalmology and Visual Science, Graduate School of Medical Sciences, Kumamoto University Kumamoto

Sponsors (1)

Lead Sponsor Collaborator
Kumamoto University

Country where clinical trial is conducted

Japan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual acuity The comparison between baseline and 12-month No
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