Renal Cancer Clinical Trial
Official title:
Kidney Cancer DNA Registry
NCT number | NCT02087852 |
Other study ID # | 13-218 |
Secondary ID | |
Status | Recruiting |
Phase | |
First received | |
Last updated | |
Start date | March 2014 |
Est. completion date | March 2026 |
Verified date | June 2024 |
Source | Memorial Sloan Kettering Cancer Center |
Contact | Jonathan Coleman, MD |
Phone | 646-422-4432 |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
This registry will help us develop better methods of: - Preventing these cancers - Diagnosing these cancers - Treating these cancers
Status | Recruiting |
Enrollment | 750 |
Est. completion date | March 2026 |
Est. primary completion date | March 2026 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: Kidney Cancer Case Cohort: - Must be = 18 years of age AND - Must be an English-speaker AND - Must have a diagnosis or suspicion of kidney cancer Family Member Cohort: - Must be = 18 years of age AND - Must be an English-speaker AND - Must be a blood relative of the proband. Family members of probands including mother, father, sisters, brothers, half-sisters, half-brothers, daughters, sons, grandmothers, grandfathers, as well as aunts and uncles are eligible. These individuals need not have kidney cancer, as they will be used for segregation analysis of suspected variants found in the proband; requesting DNA from relatives is required. Control Cohort: - Must be = 18 years of age AND - Must be an English-speaker AND - Must not have a personal history of cancer, with the exception of nonmelanoma skin cancer, AND - Must not be a blood relative of any cases or controls enrolled in this study Exclusion Criteria: - Patients who, in the opinion of the primary MSKCC clinician or the investigator, have a condition that precludes their ability to provide an informed consent |
Country | Name | City | State |
---|---|---|---|
United States | Memorial Sloan Kettering at Basking Ridge (Consent and Follow-up) | Basking Ridge | New Jersey |
United States | Memorial Sloan Kettering Commack (Consent and Follow-up) | Commack | New York |
United States | Memorial Sloan Kettering Westchester (Consent and Follow up) | Harrison | New York |
United States | Memorial Sloan Kettering Monmouth (Consent and Follow up) | Middletown | New Jersey |
United States | Memorial Sloan Kettering Bergen (Consent and Follow up ) | Montvale | New Jersey |
United States | Memorial Sloan Kettering Cancer Center (All Protocol Activities) | New York | New York |
United States | Memorial Sloan Kettering Nassau (Consent and Follow-Up) | Uniondale | New York |
Lead Sponsor | Collaborator |
---|---|
Memorial Sloan Kettering Cancer Center |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | establish a kidney cancer registry | with detailed epidemiologic data and germline DNA available for next generation sequencing from consenting patients, selected family members, and healthy unrelated controls. | 5 years |
Status | Clinical Trial | Phase | |
---|---|---|---|
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