Purpose of this Study
We are doing this study is to collect additional follow-up data and samples from participants who completed the P-RAD clinical trial.
Who Can Participate?
Eligibility
Patients who are participating or have recently participated in the P-RAD clinical trial may be included in this study.
For more information about this study, please contact the study team at <a href= "mailto: caroline.morales@duke.edu">caroline.morales@duke.edu.</a>
For more information about this study, please contact the study team at <a href= "mailto: caroline.morales@duke.edu">caroline.morales@duke.edu.</a>
Age Range
18-110
Sex/Genders
Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No
What is Involved?
If you choose to join this study, we will collect medical information about you for 3 years. You will have a yearly physical exam and review of medical history that will align with your regularly scheduled doctor's visits. You will also have a blood draw once a year while you are in the study.
Locations
Duke University Hospital
Duke Raleigh Hospital
Other
Visit Timing
Weekdays
Compensation
No
Spanish Materials Available
No
Study Details
Full Title
Long-term follow-up of patients enrolled on P-RAD or P-RAD TN(+) Trials
Principal Investigator
Susan
Dent
Protocol Number
PRO00113940
Enrollment Status
Pending Open to Enrollment