Ignite Creation Date:
2024-05-05 @ 6:34 PM
Last Modification Date:
2024-10-26 @ 9:34 AM
Study NCT ID:
NCT00503893
Status:
UNKNOWN
Last Update Posted:
2020-01-27
First Post:
2007-07-17
Brief Title:
Genetics of Wilms Tumor andor the Associated Conditions of Aniridia Hemihypertrophy and Genitourinary Anomalies
Sponsor:
MD Anderson Cancer Center
Organization:
MD Anderson Cancer Center
Study Overview
Official Title:
Genetics of Wilms Tumor andor the Associated Conditions of Aniridia Hemihypertrophy and Genitourinary Anomalies
Status:
UNKNOWN
Status Verified Date:
2020-01
Last Known Status:
ACTIVE_NOT_RECRUITING
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
The goal of this clinical research study is to collect information and blood samples to try to learn why some people develop cancers and tumors why some families have more cancers than others and whether certain genes or regions of DNA the genetic material of cells affect a persons risk of getting cancer
This is an investigational study
Up to 1500 patients and family members will take part in this study All will be enrolled at MD Anderson
This is an investigational study
Up to 1500 patients and family members will take part in this study All will be enrolled at MD Anderson
Detailed Description:
If you choose to take part in this study blood about 10 teaspoons will be drawn for genetic testing The blood may be drawn more than 1 time depending on how much blood is drawn at the first visit and if you are available for more blood draws If this is the case your doctor will discuss any extra blood draws with you
For small children less than 5 years old about 2 teaspoons will be drawn Children who are 5 years old or older will not have more than 3 teaspoons drawn
You will complete a questionnaire about your medical history and family medical history The questionnaire should take about 1 hour to complete The study staff will also review your medical records
You will be asked to allow the study staff to collect any of your tissue whether healthy or cancerous that is leftover from surgeries performed as part of your standard care This may be from any past or future surgeries or any tissue being stored at MD Anderson or elsewhere No new surgeries or biopsies will be performed for this study
Before your information tissue samples andor bodily fluids can be used for research the people doing the research must get specific approval from the Institutional Review Board IRB of MD Anderson The IRB is a committee made up of doctors researchers and members of the community The IRB is responsible for protecting the participants involved in research studies and making sure all research is done in a safe and ethical manner All research done at MD Anderson including research involving your information tissue samples andor bodily fluids must first be approved by the IRB
You may be contacted either by phone or mail 1 time a year so that the study staff can update your medical history and information If contacted by phone this call should last about 30 minutes
For small children less than 5 years old about 2 teaspoons will be drawn Children who are 5 years old or older will not have more than 3 teaspoons drawn
You will complete a questionnaire about your medical history and family medical history The questionnaire should take about 1 hour to complete The study staff will also review your medical records
You will be asked to allow the study staff to collect any of your tissue whether healthy or cancerous that is leftover from surgeries performed as part of your standard care This may be from any past or future surgeries or any tissue being stored at MD Anderson or elsewhere No new surgeries or biopsies will be performed for this study
Before your information tissue samples andor bodily fluids can be used for research the people doing the research must get specific approval from the Institutional Review Board IRB of MD Anderson The IRB is a committee made up of doctors researchers and members of the community The IRB is responsible for protecting the participants involved in research studies and making sure all research is done in a safe and ethical manner All research done at MD Anderson including research involving your information tissue samples andor bodily fluids must first be approved by the IRB
You may be contacted either by phone or mail 1 time a year so that the study staff can update your medical history and information If contacted by phone this call should last about 30 minutes
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None
Secondary IDs
| Secondary ID | Type | Domain | Link |
|---|---|---|---|
| P01CA034936-23 | NIH | None | httpsreporternihgovquickSearchP01CA034936-23 |