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Trial details imported from ClinicalTrials.gov
For full trial details, please see the original record at
https://clinicaltrials.gov/study/NCT01000753
Registration number
NCT01000753
Ethics application status
Date submitted
22/10/2009
Date registered
23/10/2009
Date last updated
3/10/2023
Titles & IDs
Public title
Collecting and Storing Tissue Samples From Patients With Rare or Cutaneous Non-Hodgkin Lymphoma
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Scientific title
Rare And Cutaneous Non-Hodgkin Lymphoma Registry
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Secondary ID [1]
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NCI-2009-00406
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Secondary ID [2]
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ANHL04B1
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Adult Immunoblastic Lymphoma
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Central Nervous System Non-Hodgkin Lymphoma
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Childhood Immunoblastic Lymphoma
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Grade 1 Follicular Lymphoma
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Grade 2 Follicular Lymphoma
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Grade 3 Follicular Lymphoma
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Lymphoproliferative Disorder
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Mantle Cell Lymphoma
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Marginal Zone Lymphoma
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Non-Hodgkin Lymphoma
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Primary Cutaneous B-Cell Non-Hodgkin Lymphoma
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Primary Cutaneous T-Cell Non-Hodgkin Lymphoma
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Small Lymphocytic Lymphoma
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Condition category
Condition code
Cancer
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Lymphoma (non Hodgkin's lymphoma) - High grade lymphoma
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Cancer
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Lymphoma (non Hodgkin's lymphoma) - Low grade lymphoma
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Cancer
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Leukaemia - Chronic leukaemia
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Cardiovascular
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Diseases of the vasculature and circulation including the lymphatic system
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Inflammatory and Immune System
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Other inflammatory or immune system disorders
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Intervention/exposure
Study type
Observational
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Patient registry
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Target follow-up duration
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Target follow-up type
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Description of intervention(s) / exposure
Other interventions - Cytology Specimen Collection Procedure
Observational (specimen collection) - See Detailed Description
Other interventions: Cytology Specimen Collection Procedure
Correlative studies
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Intervention code [1]
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Other interventions
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Comparator / control treatment
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Control group
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Outcomes
Primary outcome [1]
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Clinical features, treatment, and outcomes
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Assessment method [1]
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Timepoint [1]
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Up to 5 years
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Primary outcome [2]
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Pathologic and biologic features of these diseases, including molecular diagnostics and flow cytometry
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Assessment method [2]
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Timepoint [2]
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Up to 5 years
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Primary outcome [3]
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Establishment of a bank of these pathologically reviewed diseases and make specimens of blood and tissue available to qualified researchers
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Assessment method [3]
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Timepoint [3]
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Up to 5 years
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Primary outcome [4]
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Sub-groups of these diseases that could be targeted for future biologic, pathologic, or therapeutic studies
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Assessment method [4]
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Timepoint [4]
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Up to 5 years
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Eligibility
Key inclusion criteria
* Diagnosis of NHL
* Any histology, except for Burkitt or Burkitt-like, diffuse large B-cell, anaplastic large cell, or lymphoblastic lymphoma
* Primary CNS, primary cutaneous NHL, or lymphoproliferative diseases of any histology allowed
* Pathological specimen from site not treated within the past 6 months
* Must have specimens available
* At least 6 months since prior chemotherapy irradiation to study lesion
* At least 2 weeks since prior steroids
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Minimum age
No limit
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Maximum age
21
Years
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Sex
Both males and females
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Can healthy volunteers participate?
No
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Key exclusion criteria
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Study design
Purpose
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Duration
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Selection
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Timing
Prospective
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Statistical methods / analysis
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Recruitment
Recruitment status
Completed
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Data analysis
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Reason for early stopping/withdrawal
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Other reasons
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Date of first participant enrolment
Anticipated
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Actual
30/05/2005
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
30/09/2023
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Sample size
Target
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Accrual to date
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Final
174
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Recruitment in Australia
Recruitment state(s)
WA
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Recruitment hospital [1]
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Princess Margaret Hospital for Children - Perth
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Recruitment postcode(s) [1]
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6008 - Perth
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Recruitment outside Australia
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United States of America
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State/province [1]
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Alabama
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United States of America
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Arizona
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United States of America
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Arkansas
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United States of America
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California
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Country [5]
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United States of America
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Colorado
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Country [6]
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United States of America
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Connecticut
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Country [7]
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United States of America
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State/province [7]
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Delaware
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Country [8]
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United States of America
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State/province [8]
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District of Columbia
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Country [9]
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United States of America
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State/province [9]
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Florida
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Georgia
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United States of America
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Illinois
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Indiana
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United States of America
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Iowa
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Kansas
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Kentucky
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Louisiana
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Maine
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Maryland
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Massachusetts
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Wisconsin
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Alberta
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Canada
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British Columbia
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Canada
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Manitoba
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Canada
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Nova Scotia
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Canada
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Ontario
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Saskatchewan
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Puerto Rico
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San Juan
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Funding & Sponsors
Primary sponsor type
Other
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Name
Children's Oncology Group
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Address
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Other collaborator category [1]
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Government body
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Name [1]
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National Cancer Institute (NCI)
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Address [1]
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Ethics approval
Ethics application status
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Summary
Brief summary
This research study is collecting and storing tissue samples from patients with rare or cutaneous non-Hodgkin lymphoma. Collecting and storing samples of tissue from patients with cancer to test in the laboratory may help the study of cancer in the future.
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Trial website
https://clinicaltrials.gov/study/NCT01000753
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Amanda M Termuhlen
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Address
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Children's Oncology Group
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Phone
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Email
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Email
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Contact person for scientific queries
No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
No documents have been uploaded by study researchers.
Results not provided in
https://clinicaltrials.gov/study/NCT01000753
Download to PDF