Trials / Completed
CompletedNCT05611905
Biodistribution and Pathophysiology Study of 11C-para-aminobenzoic Acid
Phase 1 Biodistribution and Pathophysiology Study of 11C-para-aminobenzoic Acid (11C-PABA)
- Status
- Completed
- Phase
- —
- Study type
- Observational
- Enrollment
- 13 (actual)
- Sponsor
- Johns Hopkins University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- —
Summary
The investigators will perform radionuclide PET scans in subjects with infectious diseases to assess whether radio-labeled PABA (11C-PABA) is effective for infection imaging. Tomographic imaging can be used to evaluate disease processes deep within the body, noninvasively and relatively rapidly. The goal is to see if this imaging technique can help differentiate infections from non-infectious processes and also provide information on the causative bacterial class.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| COMBINATION_PRODUCT | 11C-para-aminobenzoic acid PET/CT | A bolus of 20 mCi of 11C-PABA followed by PET/CT |
| DRUG | Probenecid | Oral dose of 500 mg (tablet) 2 hours before IV dose of 11C-PABA will be administered. |
Timeline
- Start date
- 2023-12-22
- Primary completion
- 2025-11-08
- Completion
- 2025-11-08
- First posted
- 2022-11-10
- Last updated
- 2025-12-12
Locations
1 site across 1 country: United States
Regulatory
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT05611905. Inclusion in this directory is not an endorsement.