Venous Obstruction in Neurodegenerative Disorders Research Registry

This study is currently recruiting participants.
Verified May 2012 by Synergy Health Concepts, Inc.
Sponsor:
Information provided by (Responsible Party):
Synergy Health Concepts, Inc.
ClinicalTrials.gov Identifier:
NCT01593358
First received: May 5, 2012
Last updated: NA
Last verified: May 2012
History: No changes posted

May 5, 2012
May 5, 2012
August 2011
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Not Provided
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No Changes Posted
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Venous Obstruction in Neurodegenerative Disorders Research Registry
Venous Obstruction in Neurodegenerative Disorders Research Registry

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

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.

Observational
Observational Model: Case-Only
Time Perspective: Retrospective
Not Provided
Not Provided
Non-Probability Sample

Human subjects will be approached for participation in this registry that are receiving or seeking medical care at Synergy Health Concepts, Inc.No individuals shall be excluded from participation in the Research Registry based on race, ethnicity, or gender.

Chronic Cerebral Spinal Venous Insufficiency
Not Provided
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*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruiting
2000
January 2014
Not Provided

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
Both
18 Years to 90 Years
No
Contact: Frances DeBarge-Igoe, RN (949) 221-0129 uscangionurse@aol.com
United States
 
NCT01593358
RESEARCH_REGISTRY
Yes
Synergy Health Concepts, Inc.
Synergy Health Concepts, Inc.
Not Provided
Principal Investigator: John Joseph Hewett, MD Study Principal Investigator
Synergy Health Concepts, Inc.
May 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP