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

NCT01593891 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 45

Last updated 2012-05-08

No results posted yet for this study

Summary

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

Conditions

  • 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.

Sponsors & Collaborators

  • Synergy Health Concepts, Inc.

    lead INDUSTRY

Principal Investigators

  • Michael Arata, MD · Study Principal Investigator

Eligibility

Min Age
20 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-08-31
Completion
2012-09-30

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01593891 on ClinicalTrials.gov