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Study Summary
No. P80-099:.......Genitourinary; Syndrome......Louise C. Strong......Molecular Genetics
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Study Summary Title
Study Summary
Number:
P80-099
Study Title:Genetics of Wilms' Tumor and/or the Associated Conditions of Aniridia, Hemihypertrophy, and Genitourinary Anomalies
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Physician New Patient Referral
Name:Louise C. StrongPatients Call:800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Dept:Molecular GeneticsReferring MD
Call:
800-392-1611 (in U.S.A.) 713-792-6161 (outside U.S.A.)
Phone:713-792-7555
Contact us about clinical trials
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General Information
Disease Group:Genitourinary
Syndrome
Supported By:N/A
Phase of Study:N/AReturn
Visit:
Blood will be collected during routine visits to MDACC. Field trips may be
arranged so that blood from many members of the family may be drawn. There is
no reason for any participant to make a special trip back to MDACC.
Treatment
Agents:
NoneHome Care:Blood collection packs may be sent to the homes of participants. Blood will be
collected and returned to researchers.
Treatment Loc:Only at MDACC
Estimated
Length of Stay
in Houston:
None
Description/
Intervention:
The purpose of this clinical research study is to determine
· Why some people develop cancers and tumors
· Why some families have more cancers than others
· Whether certain genes or regions of DNA influence an individual's risk of
cancer
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Study Objectives / Outcomes
The overall goals are to characterize the genetic events involved in the development of Wilms' tumor, genitourinary anomalies, hemihypertrophy and Beckwith-Wiedemann, and/or aniridia by a combined molecular biology/epidemiologic approach. The study involves investigation of patients with familial and sporadic Wilms' tumor, genitourinary anomalies Beckwith-Wiedemann hemihypertrophy and/or aniridia.
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Study Status Information
Study Activation / Registration Date:
IRB Review and Approval Date:08/27/2002
Study Type:
Recruitment Status:Open
Projected Accrual:N/A
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Enrollment Eligibility
If you do not meet the enrollment eligibility, there may be other treatment options for you. Please Contact the Referral Office for more information.

Inclusion Criteria:1) Patients with familial and sporadic Wilm's tumor, genitourinary anomalies, Beckwith-Wiedemann hemihypertrophy and/or aniridia, and family members of patients.

Exclusion Criteria:1) Patients who do not meet inclusion eligilibilty criteria are excluded.

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Links
Registration Number: NCT00503893
Study Information on Clinical Trials Registry (clinicaltrials.gov)

Other Links:
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Results


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