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Hereditary Colorectal and Associated Tumor Registry Study

Hereditary Colorectal and Associated Tumor Registry Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00633607
Enrollment
114
Registered
2008-03-12
Start date
2012-04-30
Completion date
2018-01-26
Last updated
2018-02-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

FAP, Hereditary Diffuse Gastric Cancer, Juvenile Polyposis Syndrome, Lynch Syndrome, Peutz-Jeghers Syndrome

Brief summary

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.

Interventions

Information regarding medical and family history is stored in the registry to be used for potential future studies

Sponsors

University of Pittsburgh
Lead SponsorOTHER

Study design

Observational model
FAMILY_BASED
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
8 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* 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

Design outcomes

Primary

MeasureTime frame
Establish a Hereditary Colorectal Tumor Registry to facilitate development and implementation of epidemiological, clinical and cancer control research.1-N/A (up to 8 years)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026