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Completed Phase 2 Interventional Results available

Facilitated Antegrade Steering Technique in Chronic Total Occlusions (FAST-CTOs)

ClinicalTrials.gov ID: NCT00886899

Public ClinicalTrials.gov record NCT00886899. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 4:05 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Facilitated Antegrade Steering Technique in Chronic Total Occlusions

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Prospective, non-randomized, multicenter study in subjects with coronary artery chronic total occlusions (CTOs). Published results of safety and effectiveness of conventional techniques will be used for comparison. Enrollment of up to 149 subjects with a CTO refractory to currently marketed guidewire use and meeting all inclusion/exclusion criteria at up to 15 US clinical sites. Hypothesis is that the BridgePoint Medical System is safe and effective in treating coronary CTOs compared to CTO literature.

Study identification

NCT ID
NCT00886899
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
BridgePoint Medical
Industry
Enrollment
147 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 2009 (Type not available)
Primary completion
Aug 2010 (Actual)
Completion
Sep 2010 (Actual)
Last update posted
Mar 20, 2012

2009 – 2010

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
St. Luke's Medical Center Phoenix Arizona 85006 —
Scripps Clinic La Jolla California 92037 —
University of California Davis Heart & Vascular Center Sacramento California 95817 —
Stanford University Hospital Stanford California 94305 —
Torrance Memorial Medical Center Torrance California 90505 —
Yale-New Haven Hospital New Haven Connecticut 06520 —
Prairie Cardiovascular Consultants Springfield Illinois 62701 —
Minneapolis Heart Institute, Abbott Northwestern Hospital Minneapolis Minnesota 55407 —
Mayo Clinic - St. Mary's Hospital Rochester Minnesota 55905 —
Mid America Heart Institute, St. Luke's Hospital Kansas City Missouri 64111 —
Dartmouth Hitchcock Medical Center Lebanon New Hampshire 03756 —
Columbia University Medical Center New York New York 10032 —
Cleveland Clinic Cleveland Ohio 44195 —
Dallas VA Medical Center Dallas Texas 75216 —
Intermountain Medical Center Murray Utah 84157 —
St. Joseph Hospital Bellingham Washington 98225 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00886899, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 20, 2012 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00886899 live on ClinicalTrials.gov.

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