Radiographic and Intravascular (IVUS) Evaluation of Venous Morphology During CCSVI Treatment

Status unconfirmed

Conditions studied: To Determine the Safety and Validity of Venous Angioplasty and, Valvuloplasty in the Treatment of CCSVI. In Addition, it Will, Allow Researchers to Sub-classify Valve Morphology in Relation, to Treatment Success. This Will be Evidenced by Venous Patency, Forty-eight Hours by Doppler Ultrasound as Well as Clinical, Symptom Improvement.

In brief

Radio graphic and Intravascular (IVUS) Evaluation of Venous Morphology During Chronic Cerebral Spinal Venous Insufficiency Treatment

Key facts

Study ID

NCT01593891

Run by

Synergy Health Concepts, Inc.

People needed

45

Starts

2011-08-01

Expected to finish

2012-09-01

Last updated by the study team

2012-05-08

Who can join

Age: 20 and older, up to 60. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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 20 and 60 years of age.
• Voluntary agreement to participate in the study: Radiographic and Intravascular (IVUS) Evaluation of Venous Morphology During CCSVI Treatment.

You may not qualify if…

• Any implantable/metallic objects that prevents subject from having a magnetic resonance imaging (MRI/MRV) study.
• History of uncontrolled hypertension
• Previous CCSVI treatment
• Presence of hypercoagulable state
• 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.

Where it is running

• Synergy Health Concepts Inc. — Newport Beach, California, United States

Full record on ClinicalTrials.gov

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