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Correlation Between Serum Markers of Unstable Plaque and Virtual Histology of Unstable Plaque Visualized by IVUS (IVUS)

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT00466050
First Posted: April 27, 2007
Last Update Posted: August 25, 2009
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by:
Ziv Hospital
  Purpose

Thirty patients scheduled to coronary angiography and IVUS in according to their treating physician decision will be enrolled in the study. The coronary angiography and IVUS will be done on according to regular clinical standards.

As the study protocol, 40 cc of blood will be drawn from the patients after written informed consent.

The laboratory tests will be processed for the above mentioned serum markers of unstable plaque.

A multivariate correlation test will be done between the different serum markers and the plaque morphology by angiography and composition (virtual histology) by IVUS.


Condition
Acute Coronary Thrombose Plaque Rupture Acute Coronary Syndrome

Study Type: Observational
Study Design: Observational Model: Case-Only
Time Perspective: Prospective
Official Title: Correlation Between Serum Markers of Unstable Plaque and Virtual Histology of Unstable Plaque Visualized by IVUS

Further study details as provided by Ziv Hospital:

Estimated Enrollment: 30
Study Start Date: April 2007
Study Completion Date: May 2009
Primary Completion Date: April 2008 (Final data collection date for primary outcome measure)
  Show Detailed Description

  Eligibility

Information from the National Library of Medicine

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Ages Eligible for Study:   18 Years and older   (Adult, Senior)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Sampling Method:   Probability Sample
Study Population
Patients scheduled to coronary angiography and IVUS
Criteria

Inclusion Criteria:

  • Both genders: males and females
  • Age - above 18 years
  • Patients scheduled to coronary angiography and IVUS
  • Written Informed Consent Form

Exclusion Criteria:

  • Pregnant or breast-feeding woman
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00466050


Locations
Israel
Heart Institute ,Ziv Medical Center
Safed, Israel, 13110
Sponsors and Collaborators
Ziv Hospital
Investigators
Principal Investigator: Osamah Hussein, MD Ziv Medical Center
Principal Investigator: Alon Marmor, Prof Ziv Medical Center
  More Information

Publications:

Responsible Party: Ziv Hospital
ClinicalTrials.gov Identifier: NCT00466050     History of Changes
Other Study ID Numbers: HP-7-234-S
First Submitted: April 25, 2007
First Posted: April 27, 2007
Last Update Posted: August 25, 2009
Last Verified: April 2007

Keywords provided by Ziv Hospital:
plaque rupture,
acute coronary thrombose,
coronary angiography,
IVUS

Additional relevant MeSH terms:
Acute Coronary Syndrome
Rupture
Myocardial Ischemia
Heart Diseases
Cardiovascular Diseases
Vascular Diseases
Wounds and Injuries