Hereditary Colorectal and Associated Tumor Registry Study
Completed
Conditions studied: Lynch Syndrome, FAP, Hereditary Diffuse Gastric Cancer, Juvenile Polyposis Syndrome, Peutz-Jeghers Syndrome
In brief
After informed consent, participants will be asked to complete a medical/family history questionnaire and provide a blood sample. Participants will also be asked for their permission for study investigators to access medical records and/or recontact them for updates to their medical and family histories. Data and biospecimens will be stored for potential future research projects.
Key facts
- Study ID
- NCT00633607
- Run by
- University of Pittsburgh
- People needed
- 114
- Starts
- 2012-04-01
- Expected to finish
- 2018-01-26
- Last updated by the study team
- 2018-02-19
Who can join
Age: 8 and older, up to 100. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Identified gene mutation
- Personal history of colorectal cancer diagnosed ≤ 50
- Personal history of cancer with tumor studies suggestive of Lynch syndrome
- Personal history of multiple primary tumors associated with a hereditary cancer syndrome (colorectal, uterus, stomach, ovary, small bowel, hepatobiliary tract, transitional cell carcinoma of the renal pelvis/ureter, brain)
- Personal history of one of the above cancers and a family history of one or more of the above cancers
- Personal or family history of diffuse gastric cancer
- From a known genetic predisposition family
- Personal history of > 10 colon adenomas (cumulative over a lifetime)
- Personal history of any number of hamartomatous polyps
- Personal history of multiple large (> 1cm) serrated polyps to right of sigmoid
- Exclusion critera:
- Individuals under the age of 8
- Individuals who cannot travel to Pittsburgh for in-person enrollment
- Individuals who cannot provide informed consent
Where it is running
- University of Pittsburgh — Pittsburgh, Pennsylvania, United States
Full record on ClinicalTrials.gov
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