Status
Conditions
Treatments
About
This research study is creating a way to collect and store specimens and information from participants who may be at an increased risk of developing cancer, or has been diagnosed with an early phase of a cancer or a family member who has a family member with a precursor condition for cancer.
Full description
The objective of this protocol is to obtain clinical information and facilitate the collection and distribution of specimens obtained during the course of clinical care or research participation.
It is expected that about 5,000 people will take part in this research study.
Enrollment
Sex
Volunteers
Inclusion criteria
Participants to be included in this study include the following (note that this list is not comprehensive but gives examples of precursor conditions for each organ type):
1-Hereditary risk for cancer including
Exposed High Risk including
Precursor Lesions including
FAMILY MEMBERS or healthy individuals
Exclusion criteria
There are no exclusion criteria for the study.
Note: Patients with prior cancer history are allowed to participate. Patients with prior history of cancer or non-metastatic localized cancers (such as skin cancer or localized prostate cancer) are allowed to be enrolled. Patients enrolled in clinical trials or receiving therapy for precursor diseases are NOT excluded from this study.
5,000 participants in 4 patient groups
Loading...
Central trial contact
Jenna Beckwith, MPH; Tia Kauffman, MPH
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal