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Macular Function During Anti-VEGF Treatment

Study of Macular Function During Anti-VEGF Treatment

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01023971
Acronym
MAFAT
Enrollment
40
Registered
2009-12-02
Start date
2009-01-31
Completion date
Unknown
Last updated
2009-12-02

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

Conditions

Age Related Macular Degeneration

Brief summary

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

Detailed description

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

Interventions

None listed

Sponsors

Royal Liverpool University Hospital
Lead SponsorOTHER_GOV

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

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

Design outcomes

Primary

MeasureTime frame
mfERG central ring amplitude density12 months

Secondary

MeasureTime frame
Mean retinal sensitivity (dB) in three concentric rings (4°, 8° & 12°)12 months
Choroidal blood flow (ChBFlow) at fovea and at optic nerve head12 months

Countries

United Kingdom

Contacts

Primary ContactSimon P Harding, FRCOphth, MD
S.P.Harding@liverpool.ac.uk+44 0151 706
Backup ContactClaudio S Campa, MD, PhD
Claudio.Campa@rlbuht.nhs.uk+44 0151 706

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 29, 2026