NCT00640068

Brief Summary

The ACIC is a Collaborative Quality Improvement (CQI) program involving the collection of data related to: indications for Coronary Computed Tomography (CCTA), patient health characteristics, acquisition techniques of CCTA scans, physician interpretation of results and short-term outcomes over a 90 day period.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
42,926

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jul 2007

Longer than P75 for all trials

Geographic Reach
1 country

50 active sites

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

July 1, 2007

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

March 14, 2008

Completed
6 days until next milestone

First Posted

Study publicly available on registry

March 20, 2008

Completed
6 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2014

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2014

Completed
Last Updated

April 3, 2014

Status Verified

April 1, 2014

Enrollment Period

6.8 years

First QC Date

March 14, 2008

Last Update Submit

April 2, 2014

Conditions

Keywords

coronary artery diseasechest paincoronary artery bypass graftstress testCoronary Angiography

Outcome Measures

Primary Outcomes (1)

  • Educate participating sites on appropriate use of CCTA

    To educate participating sites in the clinical uses of CCTA recommended by the ACC/ACR as well as other best-practices

    5 years

Secondary Outcomes (1)

  • To monitor the CQI process of individual participating sites and the ACIC as a whole.

    5 years

Study Arms (1)

1

All patients in whom a clinical CCTA was ordered by their physician at a participating site. Patient must have a prescription for CCTA ordered by their physician.

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Referral from other healthcare provider or support staff (e.g. physician office, clinics), Emergency Room, self referral with prescription

You may qualify if:

  • (Patient must meet one criteria)
  • Patient has had a CCTA examination ordered by a referring physician at a participating site.
  • Patient is a self referral.

You may not qualify if:

  • Clinical contraindications to CCTA are present as determined by attending physician or staff, including but not limited to:
  • Pregnancy or potential pregnancy.
  • Renal failure or dysfunction.
  • Inability to receive beta blockers.
  • Allergy to iodinated contrast without prior premedication.
  • Unwillingness to participate.
  • Inability to read or understand Patient Information Sheet.
  • Age less than 18 years without parent or guardian's evaluation of Patient Information Sheet. Underage and other vulnerable populations are included as the CQI process is intended to detect and correct adverse consequences of CCTA, e.g., excessive radiation, and protect such patients.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (50)

University of Michigan

Ann Arbor, Michigan, 48109, United States

Location

St. Joseph Mercy Hospital Ann Arbor

Ann Arbor, Michigan, 48706, United States

Location

Bay Regional Medical Center

Bay City, Michigan, 48708, United States

Location

DMC Huron Valley-Sinai

Commerce, Michigan, 48382, United States

Location

Oakwood Hospital

Dearborn, Michigan, 48124, United States

Location

Harper University Hospital

Detroit, Michigan, 48201, United States

Location

Henry Ford Hospital

Detroit, Michigan, 48202, United States

Location

St. John Hospital and Medical Center

Detroit, Michigan, 48236, United States

Location

McLaren Flint

Flint, Michigan, 48532, United States

Location

McLaren Regional Medical Center

Flint, Michigan, 48532, United States

Location

Premier Medical Clinics

Flint, Michigan, 48532, United States

Location

Garden City Hospital

Garden City, Michigan, 48135, United States

Location

North Ottawa Community Hospital

Grand Haven, Michigan, 49417, United States

Location

East Beltline Imaging

Grand Rapids, Michigan, 49525, United States

Location

Henry Ford Cottage Hospital

Grosse Pointe, Michigan, 48043, United States

Location

William Beaumont Hospital - Grosse Pointe

Grosse Pointe, Michigan, 48230, United States

Location

Hillsdale Community Health Center

Hillsdale, Michigan, 49242, United States

Location

Bronson Hospital

Kalamazoo, Michigan, 49007, United States

Location

Borgess Medical Center

Kalamazoo, Michigan, 49048, United States

Location

Sparrow Health System

Lansing, Michigan, 48909, United States

Location

Ingham Regional Medical Center

Lansing, Michigan, 48910, United States

Location

Thoracic and Cardiovascular Institute, P.C.

Lansing, Michigan, 48910, United States

Location

McLaren Lapeer Region

Lapeer, Michigan, 48446, United States

Location

St. John Oakland

Madison Heights, Michigan, 48071, United States

Location

Marquette General Health System

Marquette, Michigan, 49855, United States

Location

Mercy Memorial

Monroe, Michigan, 48162, United States

Location

McLaren Macomb

Mount Clemens, Michigan, 48043, United States

Location

Hackley Hospital

Muskegon, Michigan, 49442, United States

Location

Northern Michigan Hospital

Petoskey, Michigan, 49770, United States

Location

Pontiac Osteopathic Hospital

Pontiac, Michigan, 48124, United States

Location

St. Joseph Mercy Hospital Oakland

Pontiac, Michigan, 48341, United States

Location

Crittenton Hospital

Rochester, Michigan, 48307, United States

Location

William Beaumont Hospital-Royal Oak

Royal Oak, Michigan, 48073, United States

Location

Covenant Healthcare

Saginaw, Michigan, 48602, United States

Location

Lakeland Regional Health System

Saint Joseph, Michigan, 49085, United States

Location

Chippewa County War Memorial

Sault Saint Marie, Michigan, 49783, United States

Location

St. John Providence Hospital

Southfield, Michigan, 48075, United States

Location

Southgate Radiology & Southgate CT

Southgate, Michigan, 48195, United States

Location

St. Joseph Health System - Tawas

Tawas City, Michigan, 48764, United States

Location

Heritage (Oakwood) Hospital

Taylor, Michigan, 48180, United States

Location

Munson Medical Center

Traverse City, Michigan, 49684, United States

Location

Oakwood Southshore Medical Center

Trenton, Michigan, 48183, United States

Location

William Beaumont Hospital, Troy

Troy, Michigan, 48085-1117, United States

Location

St. John Macomb

Warren, Michigan, 48093, United States

Location

Oakwood Annapolis Hospital

Wayne, Michigan, 48184, United States

Location

Henry Ford West Bloomfield Hospital

West Bloomfield, Michigan, 48322, United States

Location

Health First Imaging

West Bloomfield, Michigan, 48323, United States

Location

West Branch Regional Medical Center

West Branch, Michigan, 48661, United States

Location

Henry Ford Wyandotte Hospital

Wyandotte, Michigan, 48192, United States

Location

Michigan Heart, P.C.

Ypsilanti, Michigan, 48197, United States

Location

Related Publications (6)

  • Burris AC 2nd, Boura JA, Raff GL, Chinnaiyan KM. Triple Rule Out Versus Coronary CT Angiography in Patients With Acute Chest Pain: Results From the ACIC Consortium. JACC Cardiovasc Imaging. 2015 Jul;8(7):817-25. doi: 10.1016/j.jcmg.2015.02.023. Epub 2015 Jun 17.

  • Chinnaiyan KM, Boura JA, DePetris A, Gentry R, Abidov A, Share DA, Raff GL; Advanced Cardiovascular Imaging Consortium Coinvestigators. Progressive radiation dose reduction from coronary computed tomography angiography in a statewide collaborative quality improvement program: results from the Advanced Cardiovascular Imaging Consortium. Circ Cardiovasc Imaging. 2013 Sep;6(5):646-54. doi: 10.1161/CIRCIMAGING.112.000237. Epub 2013 Aug 7.

  • Chinnaiyan KM, Depetris AM, Al-Mallah M, Abidov A, Ananthasubramaniam K, Gallagher MJ, Girard S, Goraya TY, Kazerooni EA, Patel S, Peyser P, Poopat C, Raff GL, Saba S, Song T, Share D. Rationale, design, and goals of the Advanced Cardiovascular Imaging Consortium (ACIC): A Blue Cross Blue Shield of Michigan collaborative quality improvement project. Am Heart J. 2012 Mar;163(3):346-53. doi: 10.1016/j.ahj.2011.11.018.

  • Chinnaiyan KM, Raff GL, Goraya T, Ananthasubramaniam K, Gallagher MJ, Abidov A, Boura JA, Share D, Peyser PA. Coronary computed tomography angiography after stress testing: results from a multicenter, statewide registry, ACIC (Advanced Cardiovascular Imaging Consortium). J Am Coll Cardiol. 2012 Feb 14;59(7):688-95. doi: 10.1016/j.jacc.2011.10.886.

  • Vanhecke TE, Madder RD, Weber JE, Bielak LF, Peyser PA, Chinnaiyan KM. Development and validation of a predictive screening tool for uninterpretable coronary CT angiography results. Circ Cardiovasc Imaging. 2011 Sep;4(5):490-7. doi: 10.1161/CIRCIMAGING.111.964205. Epub 2011 Jul 20.

  • Raff GL, Chinnaiyan KM, Share DA, Goraya TY, Kazerooni EA, Moscucci M, Gentry RE, Abidov A; Advanced Cardiovascular Imaging Consortium Co-Investigators. Radiation dose from cardiac computed tomography before and after implementation of radiation dose-reduction techniques. JAMA. 2009 Jun 10;301(22):2340-8. doi: 10.1001/jama.2009.814.

MeSH Terms

Conditions

Chest PainCoronary OcclusionCoronary Artery Disease

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and SymptomsCoronary DiseaseMyocardial IschemiaHeart DiseasesCardiovascular DiseasesVascular DiseasesArteriosclerosisArterial Occlusive Diseases

Study Officials

  • Kavitha Chinnaiyan, MD

    Corewell Health East

    STUDY DIRECTOR

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Medical Director of Noninvasive Cardiology Education; Program Director, ACIC

Study Record Dates

First Submitted

March 14, 2008

First Posted

March 20, 2008

Study Start

July 1, 2007

Primary Completion

April 1, 2014

Study Completion

April 1, 2014

Last Updated

April 3, 2014

Record last verified: 2014-04

Locations