New eye scan could Fine-Tune treatment timing for wet AMD
NCT ID NCT02868086
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at two ways of monitoring wet age-related macular degeneration (AMD) using eye scans: standard OCT B-scans and a newer technique called OCT angiography. The goal was to see if the newer scan could better detect when the disease is active, helping doctors decide when to give anti-VEGF injections. Sixty-eight adults with wet AMD were followed to compare how each scan affected treatment timing and vision stability.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If OCT angiography proves better at detecting when wet AMD is active, it could help doctors time anti-VEGF injections more precisely, potentially preserving vision with fewer visits.
- What could go wrong
- This is a small, completed study (68 people) comparing imaging techniques, not testing a new treatment. The results may not change current practice or improve vision outcomes significantly.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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68 people
The number who actually took part.
- Started
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Oct 2016
- Finished
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Apr 2021
- Lead sponsor
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A research network
The lead sponsor is a research network or cooperative group.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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50 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adult patient ≥ 50 years old * with exudative ARMD, * treated with intra-vitreous anti-angiogenics following a PRN protocol (pro re nata) * Absence of atrophy of the central pigment epithelium Exclusion Criteria * Opposition to participate in this research * Persons enjoying legal protection measure * Lack of affiliation to social security and universal health coverage * Pregnant or lactating * Another cause of Choroidal neovascularization * Unbalanced glaucoma * Eye surgery less than 3 months on the studied eye
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Fondation Ophtalmologique A. de Rotchschild
Paris, 75019, France
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- A window into the eye: could functional tests predict macular degeneration progression?
- Can a VR maze reveal hidden vision loss in macular degeneration?
- Can a new eye injection save vision in wet AMD?
- A new eye camera may spot stressed cells before vision loss begins