MINDS-CAD: Multicenter Study Into Individualized Scanning for Coronary Artery Disease

Sponsor
Medical University of South Carolina (Other)
Overall Status
Recruiting
CT.gov ID
NCT04837846
Collaborator
(none)
300
1
21.1
14.2

Study Details

Study Description

Brief Summary

To evaluate intravascular attenuation of the coronary arteries and image quality in an individualized scan and CM injection protocol whereas both scan and injection parameters are tailored to the individual patient in a North American, European and Asian patient population.

To evaluate the radiation dose and contrast media dose of this individualized approach for CCTA in an American, European and Chinese patient population.

To evaluate the injection parameters required for an average American, European and Chinese patient population.

Condition or Disease Intervention/Treatment Phase
  • Other: Differing Tube Voltage Administration

Study Design

Study Type:
Observational
Anticipated Enrollment :
300 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
Multicenter Study Into Individualized Scanning for Coronary Artery Disease
Actual Study Start Date :
Mar 29, 2021
Anticipated Primary Completion Date :
Dec 31, 2022
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Prospective CCTA Arm

Other: Differing Tube Voltage Administration
Subjects will undergo CCTA utilizing a scan and contrast media injection protocol that will be tailored to individual body habitus.

Outcome Measures

Primary Outcome Measures

  1. Evaluation of Intravascular Attenuation [At time of CCTA scan]

    To measure the amount of Hounsfield units in different anatomical structures produced by an amount of contrast media. Using Hounsfield units coupled with image quality to determine if a scan of diagnostic value has been attained.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • To be eligible for the study: (All answers must be "YES" for subject to be eligible.)
  1. Referred for a clinically indicated CCTA scan.

  2. Patient aged older than 18.

  3. Subject must provide written informed consent prior to any study-related procedures being performed.

  4. Subject must be willing to comply with all clinical study procedures.

  5. Atypical or typical complaints of angina.

  6. No previous cardiovascular history.

  7. Possibility of 'flash' mode scan; patient heart rate below 70 beats per minute and regular rhythm.

Exclusion Criteria:
  • The presence of the following excludes subjects from the study: (All answers must be "NO" for subject to be eligible.)
  1. Contraindications for CT coronary angiography, including:

  2. Inability to perform a breath hold for at least the expected scan time

  3. Unstable angina

  4. Hemodynamic instability

  5. Known history of CAD

  6. Pregnancy

  7. Renal insufficiency (defined as Creatinine <1.5 mg/dL or GFR<30 mL/min)

  8. Iodine allergy

  9. Insufficient cannula venous access (preferred 18G, minimal 20G cannula)

  10. Subject has an acute psychiatric disorder.

  11. Subject is unwilling to comply with the requirements of the protocol.

  12. Subject has previously entered this study.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Medical University of South Carolina Charleston South Carolina United States 29425

Sponsors and Collaborators

  • Medical University of South Carolina

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
U. Joseph Schoepf, MD, Professor, Medical University of South Carolina
ClinicalTrials.gov Identifier:
NCT04837846
Other Study ID Numbers:
  • 00093255
First Posted:
Apr 8, 2021
Last Update Posted:
Apr 25, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Yes
Plan to Share IPD:
Yes
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 25, 2022