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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT00584714
Other study ID # 127-014-A
Secondary ID
Status Terminated
Phase N/A
First received December 20, 2007
Last updated July 1, 2008
Start date October 2007
Est. completion date July 2008

Study information

Verified date July 2008
Source Point Biomedical
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Observational

Clinical Trial Summary

The purpose of this study is to collect longer term follow-up information concerning health and survival on selected patients who received PB127 for injectable suspension in the pivotal trial (127-014).


Recruitment information / eligibility

Status Terminated
Enrollment 300
Est. completion date July 2008
Est. primary completion date July 2008
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

Patients enrolled in Protocol 127-014 who

1. Were enrolled in Stratum 1

2. Did not undergo angiography during study evaluation

3. Did not have a clinical oucome during the initial 6 month follow-up period as described in Protocol 127-014.

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Locations

Country Name City State
United States Androscoggin Cardiovascular Associates Auburn Maine
United States Austin Heart Austin Texas
United States Seton Healthcare Network Brackenridge Hospital Austin Texas
United States Brigham & Women's Hosptial Boston Massachusetts
United States Connecticut Clinical Research Bridgeport Connecticut
United States Cardiovascular Associates of the Peninsula Burlingame California
United States Northwestern University Feinberg School of Medicine Chicago Illinois
United States The Cleveland Clinic Foundation Department of Cardiology Cleveland Ohio
United States Ohio State University College of Medicine and Public Health Columbus Ohio
United States Henry Ford Hospital Detroit Michigan
United States Duke University Medical Center Durham North Carolina
United States Consultants in Cardiology Fort Worth Texas
United States University of Texas Division of Cardiology Galveston Texas
United States Carolina Cardiology Associates High Point North Carolina
United States Methodist DeBakery Heart Center Cardiovascular Imaging Institute Houston Texas
United States University of Texas Health Science Center Memorial Hermann Heart & Vascular Institute Houston Texas
United States Cardiovascular Consultants Kansas City Missouri
United States Long Beach VA Medical Center Cardiology Division Long Beach California
United States Cedars Sinai Medical Center Division of Cardiology Los Angeles California
United States North Shore University Hospital Manhasset New York
United States St. Luke's Roosevelt Hospital Echocardiography Lab New York New York
United States Alfieri Cardiology Newark Delaware
United States Midwest Cardiology Associates Overland Park Kansas
United States Western Baptist Hospital The Heart Group Paducah Kentucky
United States University of Pittsburgh Cardiovascular Institute Pittsburgh Pennsylvania
United States Mayo Clinic Department of Cardiology Rochester Minnesota
United States Sutter Roseville Medical Center Roseville California
United States University of California San Diego Division of Cardiology San Diego California
United States San Francisco VA Medical Center NCIRE San Francisco California
United States Harborview Medical Center Department of Cardiology Seattle Washington
United States The Center for Cardiovascular Studies Kramer & Crouse Cardiology Shawnee Mission Kansas
United States Maine Cardiology Associates South Portland Maine
United States Heart Clinics Northwest Spokane Washington
United States Inland Cardiology Spokane Washington
United States Northwest Cardiovascular Research Institute Spokane Cardiology Spokane Washington
United States St. Louis University Medical Center St. Louis Missouri
United States Stonybrook University Medical Center Stonybrook New York
United States University of Arizona Saver Heart Clinic Tucson Arizona
United States Washington Hospital Center Cardiovascular Research Institute Washington District of Columbia

Sponsors (1)

Lead Sponsor Collaborator
Point Biomedical

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary To collect longer-term follow-up clinical information on selected patients enrolled in Protocol 127-014 1 year No
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