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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01023971
Other study ID # Trust R&D_3704
Secondary ID
Status Recruiting
Phase N/A
First received December 1, 2009
Last updated December 1, 2009
Start date January 2009

Study information

Verified date December 2009
Source Royal Liverpool University Hospital
Contact Simon P Harding, FRCOphth, MD
Phone +44 0151 706
Email S.P.Harding@liverpool.ac.uk
Is FDA regulated No
Health authority United Kingdom: National Health Service
Study type Observational

Clinical Trial Summary

The purpose of this study is to determine the changes in macular function during anti-VEGF treatment for neovascular age-related macular degeneration.


Description:

Macular function will be investigated using visual acuity, contrast sensitivity, mfERG and microperimetry.


Recruitment information / eligibility

Status Recruiting
Enrollment 40
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 50 Years and older
Eligibility Inclusion Criteria:

- Neovascular AMD in first or second eyes

- angiographic signs of active subfoveal or juxtafoveal choroidal neovascularization (CNV)

- BCVA =35 ETDRS letters

Exclusion Criteria:

- Spherical equivalent = ± 6 D

- Previous treatments for CNV in the studied eye

Study Design

Observational Model: Cohort, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
United Kingdom Clinical Eye Research Centre Liverpool

Sponsors (1)

Lead Sponsor Collaborator
Royal Liverpool University Hospital

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary mfERG central ring amplitude density 12 months No
Secondary Mean retinal sensitivity (dB) in three concentric rings (4°, 8° & 12°) 12 months No
Secondary Choroidal blood flow (ChBFlow) at fovea and at optic nerve head 12 months No
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