Other Clinical Trial - VEGF & PEDF in Patients With Myopic Choroidal

Clinical Trial Description

n/a

Study Design

Observational Model: Case Control, Time Perspective: Prospective

See also
Status	Clinical Trial	Phase
Completed	`NCT04524910` - A Study to Learn More About How Drug Aflibercept Works in Canadian Patients With Reduced Vision Caused by New Blood Vessels Growing in the Eye (Myopic Choroidal Neovascularization or mCNV)
Active, not recruiting	`NCT01246089` - Ranibizumab for Myopic Neovascularization	Phase 4
Completed	`NCT00797992` - Bevacizumab Intravitreal for Myopic Choroidal Neovascularization	Phase 4

See also

Status

Clinical Trial

Phase

Completed

NCT04524910 - A Study to Learn More About How Drug Aflibercept Works in Canadian Patients With Reduced Vision Caused by New Blood Vessels Growing in the Eye (Myopic Choroidal Neovascularization or mCNV)

Active, not recruiting

NCT01246089 - Ranibizumab for Myopic Neovascularization

Phase 4

Completed

NCT00797992 - Bevacizumab Intravitreal for Myopic Choroidal Neovascularization

Phase 4

Interventional studies are often prospective and are specifically tailored to evaluate direct impacts of treatment or preventive measures on disease.

Observational studies are often retrospective and are used to assess potential causation in exposure-outcome relationships and therefore influence preventive methods.

Expanded access is a means by which manufacturers make investigational new drugs available, under certain circumstances, to treat a patient(s) with a serious disease or condition who cannot participate in a controlled clinical trial.

Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

NCT number	NCT02175940
Study type	Observational
Source	Università degli Studi di Brescia
Contact
Status	Completed
Phase	N/A
Start date	July 2013
Completion date	May 2014

VEGF and PEDF in Patients With Myopic Choroidal Neovascularization

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms