Other Clinical Trial - Follow-up Study to Assess Visual Function in Subset

Clinical Trial Description

Non-interventional follow up study consisting of 1 patient visit to perform assessments to assess long term visual function ;

Study Design

Related Conditions & MeSH terms

Symptomatic Vitreomacular Adhesion

See also
	Status	Clinical Trial	Phase
	Completed	`NCT02079883` - Ocriplasmin Research to Better Inform Treatment (ORBIT)	N/A
	Completed	`NCT01889251` - A Phase III Study of A01016 in Subjects With Symptomatic Vitreomacular Adhesion	Phase 3

See also

Status

Clinical Trial

Phase

Completed

NCT02079883 - Ocriplasmin Research to Better Inform Treatment (ORBIT)

N/A

Completed

NCT01889251 - A Phase III Study of A01016 in Subjects With Symptomatic Vitreomacular Adhesion

Phase 3

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	NCT01287988
Study type	Observational
Source	ThromboGenics
Contact
Status	Completed
Phase	N/A
Start date	May 2011
Completion date	October 2011

Follow-up Study to Assess Visual Function in Subset of Patients Who Have Previously Participated in the TG-MV-006 and TG-MV-007 Ocriplasmin Studies

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms