BridgeMD
New treatment option for Healthy (Controls)
Official title Ultralow Dose PET Imaging of SSTR2 Radiotracer Uptake
ClinicalTrials.gov ID: NCT07284589
What this study is testing
What is 68Ga-Dotatate?
68Ga-Dotatate is an investigational medicine, being studied as a potential treatment for healthy (controls).
Also referred to as CT scan, PET scan.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- The goal of this clinical trial is to evaluate an investigational ultralow dose positron emission tomography (PET) imaging technique for neuroendocrine tumor detection and monitoring. The main question it aims to answer is: Can the investigators optimize the timing, scan duration, and image reconstruction to reduce the radiation dose 10-100 fold of the current clinical standard?
- Phase 2: a mid-size study of how well it works
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 to 120. Healthy volunteers may be eligible.
You may be able to join if
- Age ≥18 years.
- Ability to provide informed consent and comply with study procedures.
- For female participants: Must not be pregnant or breastfeeding; Negative pregnancy test required for women of childbearing potential.
You likely can't join if
- Participants who have exceeded NRC regulation for annual radiation exposure from prior research-related scans, including this study (50 millisievert...
- More than four prior enrollments in this study.
- Participants with severe claustrophobia, chronic pain, or musculoskeletal conditions that prevent completion of the PET scan
- Medication \& Prior Treatment Exclusions: SSTR targeted therapies
- Pregnant or breastfeeding individuals (negative pregnancy test required)
- Inability to provide informed consent
See the full eligibility criteria
- Age ≥18 years.
- Ability to provide informed consent and comply with study procedures.
- For female participants: Must not be pregnant or breastfeeding; Negative pregnancy test required for women of childbearing potential.
- Participants who have exceeded NRC regulation for annual radiation exposure from prior research-related scans, including this study (50 millisievert [mSv] total).
- More than four prior enrollments in this study.
- Participants with severe claustrophobia, chronic pain, or musculoskeletal conditions that prevent completion of the PET scan
- Medication \& Prior Treatment Exclusions: SSTR targeted therapies
- Pregnant or breastfeeding individuals (negative pregnancy test required)
- Inability to provide informed consent
- Any condition that, in the investigator's judgment, may compromise participant safety or study integrity.
The study team makes the final eligibility decision.
Where it's taking place
- Englewood, New Jersey, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years to 120 years. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Englewood, New Jersey, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.