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VEGF and PEDF in Patients With Myopic Choroidal Neovascularization

U

Università degli Studi di Brescia

Status

Completed

Conditions

VEGF Aqueous Level
Myopic Choroidal Neovascularization
PEDF Aqueous Level

Study type

Observational

Funder types

Other

Identifiers

NCT02175940
VEGF001

Details and patient eligibility

About

This was a prospective, case-control study investigating aqueous levels of VEGF and PEDF in eyes with mCNV treated with IVB.

Enrollment

40 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • pathologic myopia, defined as spherical equivalent >6 diopters and axial length >26 mm
  • posterior pole myopic retinal changes (posterior staphyloma, chorioretinal atrophy, papillary crescent);
  • fluorescein angiography, indocyanine green angiography and optical coherence tomography detection of the subfoveal or juxtafoveal choroidal neovascularization
  • clear ocular media;

Exclusion criteria

  • previous treatment for choroidal neovascularization, including the previous intravitreal drug injection or PDT
  • presence of other maculopathy as diabetic retinopathy or retinal vascular occlusion
  • history of recent myocardial infarction or other thromboembolic events
  • ongoing uncontrolled hypertension or glaucoma
  • refractive media opacities
  • previous eye surgery

Trial design

40 participants in 2 patient groups

Myopic Choroidal Neovascularization patients
Control patients undergoing cataract surgery

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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