Find the HeartFlow Analysis at a location near you with our new HeartFlow Finder tool!

close button

HeartFlow is eager to work with active clinical research sites and investigators to ensure sustainable and robust growth of our clinical programs. If you are an active researcher interested in HeartFlow’s ongoing or upcoming clinical trials, please complete the Clinical Research Site Survey. Information you provide will go into our investigator database as a resource for potential site selection.

1

Section 1 of 5
2

Section 2 of 5
3

Section 3 of 5
4

Section 4 of 5
5

Section 5 of 5
SECTION 1 OF 5


SECTION 2 OF 5

Investigator and Staff Background:

2.Are you and your staff trained on ICH GCP guidelines for conducting clinical trials?

3. Are you involved in any ongoing research studies at your site?

4. How many upcoming studies are planned in the foreseeable future?
5.Is the study coordinator assigned to more than one study?


6.Have you ever worked with Electronic Data Capture (EDC) before?

7.Do you have any experience with HeartFlow products? Please select all that apply.
VMware device used to upload DICOM case data sent from your PACS to the HeartFlow Cloud.
How many, of these specialists, review:
10. Is your site currently performing coronary CTA on patients in the emergency department?


SECTION 3 OF 5

Facilities, Equipment, and Storage Requirements:

12. What type (make and model) of CT scanner are you using?
General Electric:
Phillips:
Siemens:
Toshiba:
Hitachi:
Other:
13.Have you used any other type of CT scanner in the past 10 years?

15.Will your institution be able to deploy the HeartFlow Connect Virtual appliance to transfer CT data through a secure method?


VMware device used to upload DICOM case data sent from your PACS to the HeartFlow Cloud.
SECTION 4 OF 5

Institutional Review Board/Ethical Committee Information:

16.Is your site a single center or multi-center?

17.Can you use a central IRB/EC?

IRB/EC Site Contact(s):
18.Have you or your site ever received a warning letter from your local regulatory authority or any other auditing group regarding violations of relevant regulations?

19.Are there other requirements imposed by any other agencies or authorities in order to conduct research at your site (for example, a radiation exposure committee or scientific review committee)?

20.Will your institution be able to provide anonymized patient data required for the study?

SECTION 5 OF 5

Other:

21. What are your research areas of interest? (Check all that apply):
22. Has your site ever worked on a clinical trial with the following study design(s)? (Check all that apply)
23. What is your objective in participating in research?




1
2
3
4
5
Save to continue later