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Clinical Trial Details — Status: Withdrawn

Administrative data

NCT number NCT03494335
Other study ID # RP0320_S02/2018E0141
Secondary ID
Status Withdrawn
Phase
First received
Last updated
Start date August 30, 2022
Est. completion date December 31, 2024

Study information

Verified date January 2024
Source University of Cincinnati
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

In this exploratory study, the researchers would like to investigate the background, perception, current use practices, potential unmet needs and/or challenges in regard to imaging procedures, imaging technology, or any other aspect related to the broader field of imaging.


Description:

The researchers plan to include volunteer participants to complete these surveys. The goal of these exploratory efforts will be to increase the currently very limited information available in the topics of interest stated above, and the findings, even if only from limited group of respondents, will help guide research development, prepare for design of clinical trials, guide special interest groups, and serve as role data for appropriate scientific publications.


Recruitment information / eligibility

Status Withdrawn
Enrollment 0
Est. completion date December 31, 2024
Est. primary completion date December 31, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Male and female participants who have access to the online survey tool and can read and write in English Exclusion Criteria: - None, as this is voluntary

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Online surveys
The investigators are recruiting health care providers for these surveys that are involved in or use imaging.

Locations

Country Name City State
United States Martha Morehouse Medical Plaza Columbus Ohio

Sponsors (1)

Lead Sponsor Collaborator
University of Cincinnati

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Perception of PET/CT imaging agent Y-90 To evaluate participants' perceptions of Y-90 using a likert scale on an online survey through study completion, on average 2-5 years
Primary Perception of PET/CT imaging agent NaF To evaluate participants' perceptions of NaF using a likert scale on an online survey through study completion, on average 2-5 years
Primary Perception of MRI contrast agents To evaluate participants' perceptions of MR contrast agents using a likert scale through study completion, on average 2-5 years