Evaluation of the Veriton SPECT/CT System
Purpose
The main purpose of this study is to evaluate a new type of gamma camera (the Veriton system) that provides a significant gain in system sensitivity and improved image quality compared to a conventional gamma camera that can achieve equal or better image quality than a standard SPECT/CT system.
Condition
- Focus of Study is Comparison of 2 Types of Gamma Cameras
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Adults age 18 years or older. - Currently scheduled to undergo a nuclear medicine exam.
Exclusion Criteria
- Individuals under 18 years of age. - Unwilling/unable to sign an informed consent form. - Unable to lie on a Veriton imaging table for up to 40 minutes.
Study Design
- Phase
- N/A
- Study Type
- Interventional
- Allocation
- N/A
- Intervention Model
- Single Group Assignment
- Intervention Model Description
- each patient will have 2 scans - one on a conventional system and one on the newer technology
- Primary Purpose
- Diagnostic
- Masking
- None (Open Label)
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
|
Experimental Evaluation of the Veriton SPECT/CT system |
To determine if the Veriton system can achieve equal or better image quality than a standard SPECT/CT system. |
|
Recruiting Locations
Mayo Clinic in Rochester
Rochester, Minnesota 55905
Rochester, Minnesota 55905
More Details
- NCT ID
- NCT04722185
- Status
- Recruiting
- Sponsor
- Mayo Clinic