Other Clinical Trial - Doppler Sonography, MR Venography, Plethysmography

Clinical Trial Description

n/a

Study Design

Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

Chronic Cerebrospinal Venous Insufficiency
Venous Insufficiency

See also
	Status	Clinical Trial	Phase
	Suspended	`NCT01205633` - Multi-center Registry for CCSVI Testing and Treatment	N/A
	Withdrawn	`NCT01555684` - Functional Changes Following Percutaneous Venoplasty in Multiple Sclerosis Patients	N/A

See also

Status

Clinical Trial

Phase

Suspended

NCT01205633 - Multi-center Registry for CCSVI Testing and Treatment

N/A

Withdrawn

NCT01555684 - Functional Changes Following Percutaneous Venoplasty in Multiple Sclerosis Patients

N/A

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	NCT01425554
Study type	Interventional
Source	Euromedic Specialist Clinics, Poland
Contact
Status	Completed
Phase	N/A
Start date	August 2011
Completion date	December 2013

Doppler Sonography, MR Venography, Plethysmography for the Diagnosis of CCSVI

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms