Venous Obstruction in Neurodegenerative Disorders Research Registry

Chronic Cerebral Spinal Venous Insufficiency Clinical Trial

Official title:

Venous Obstruction in Neurodegenerative Disorders Research Registry

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT01593358
• Other study ID #: RESEARCH_REGISTRY
• Status: Recruiting
• Phase: N/A
• First received: May 5, 2012
• Last updated: May 5, 2012
• Start date: August 2011
• Est. completion date: January 2014

Study information

• Verified date: May 2012
• Source: Synergy Health Concepts, Inc.
• Contact: Frances DeBarge-Igoe, RN
• Phone: (949) 221-0129
• Email: uscangionurse[@]aol.com
• Is FDA regulated: No
• Health authority: United States: Institutional Review Board
• Study type: Observational

Clinical Trial Summary

To establish if there are venous obstructions in patients with neurodegenerative disorders

Description:

This research registry will observe the venous obstruction in neurodegenerative disorders. This will provide data that will allow researchers to classify abnormal valve and venous morphology, distinguish vessels which are more responsive to treatment, determine groups who respond more favorably to treatment, and overall evaluate the outcomes of venous angioplasty in various neurodegenerative disorders that involve venous obstruction.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 2000
• Est. completion date: January 2014
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 90 Years

Eligibility

Inclusion Criteria:

• Ability to comprehend the nature of the study, including the risks and benefits and execute an informed consent

• Males or Females between the ages of 18 and 90 years of age

• Voluntary agreement to participate in the Venous Obstructions in Neurodegenerative Diseases Research Registry

Exclusion Criteria:

• Any implantable/metallic objects that prevent subject from having a magnetic resonance imaging ( MRI/MRV) study

• History of uncontrolled hypertension

• Previous venous angioplasty treatment for Chronic cerebral spinal venous insufficiency

• Special Populations. Special groups include, but are not limited to children, prisoners, pregnant women,fetuses, and cognitively impaired individuals who are unable to provide informed consent

Study Design

Observational Model: Case-Only, Time Perspective: Retrospective

Related Conditions & MeSH terms

• Chronic Cerebral Spinal Venous Insufficiency
• Neurodegenerative Diseases
• Venous Insufficiency

Locations

Country	Name	City	State
United States	Synergy Health Concepts, Inc.	Newport Beach	California

Sponsors (1)

Lead Sponsor	Collaborator
Synergy Health Concepts, Inc.

Country where clinical trial is conducted

United States, 

External Links

•   CCSVI Alliance Website