Biomarkers and Choroidal Neovascularization

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorInstitut National de la Santé Et de la Recherche Médicale, France

About this trial

The aim of the study is to find biomarkers in the blood and aqueous humor of patients with type 1 choroidal neovascularization and correlate them with the response to anti-VEGF treatment.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients with type 1 choroidal neovascularization in a context of central serous chorioretinoathy or age related macular degeneration

Patients without intravitreal injection or last intravitreal injection > 3 months

Informed signed consent

Patients without choroidal neovascularization

Disqualifiers

Myocardial infarction < 12 months

Chronic renal failure

Inflammatory disease

Infectious disease :HIV, viral hepatitis, tuberculosis

Trial population

Group 1 : patients with type 1 choroidal neovascularization Group 2: patients without choroidal neovascularization before ocular surgery

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Blood and aqueous humor biomarker of treatment response

    Other intervention

    Blood analyses and aqueous humor analysis

Treatment groups

250 Participants
are divided into 2 treatment groups
Group A: Group 11 intervention
Group B: Group 21 intervention

Trial outcomes

Primary outcomes

1

biomarker analysis in blood and aqueous humor of patients with neovascularization and controls

Biomarker concentrations (pg/ml) will be evaluated with ELISA (Enzyme Linked ImmunoSorbent Assay).

Time frame
24 months
2

biomarker analysis in blood and aqueous humor of patients with neovascularization and controls

Biomarker concentrations (pg/ml) will be evaluated with Mulitplex Biorad.

Time frame
24 months

Secondary outcomes

1

biomarkers and treatment response

Correlation between biomarker level and the response to anti-VEGF treatment

Time frame
24 months

Other outcomes

Sponsors and contacts

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