- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00398177
Clinical and Pathologic Studies in Non-Hodgkin's Lymphoma and Hodgkin's Disease
November 21, 2023 updated by: Stanford University
The purpose of this study is to characterize the molecular and cell biology of the tumor cells in lymphoma.
Study Overview
Status
Recruiting
Conditions
Detailed Description
This research involves the study of lymphoma cells in order to better understand how the disease grows and spreads.
This study may lead to the development of special materials that could be used, in the future, to treat lymphoma or to follow the response of lymphoma to treatment.
Study Type
Observational
Enrollment (Estimated)
9999
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Ami Okada
- Phone Number: 650-725-4968
- Email: amio@stanford.edu
Study Locations
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California
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Stanford, California, United States, 94305
- Recruiting
- Stanford University School of Medicine
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Contact:
- Ami Okada
- Phone Number: 650-725-4968
- Email: amio@stanford.edu
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Sub-Investigator:
- Gideon Gross
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Sub-Investigator:
- Shoshana Levy
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Principal Investigator:
- Ronald Levy
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Sampling Method
Non-Probability Sample
Study Population
Any type of NHL or Hodgkin's disease.
Description
Inclusion Criteria:
- Diagnosis of Hodgkin's disease or non-Hodgkin's lymphoma, any cellular classification, any stage, any grade.
- Adult or pediatric patients receiving lymph node excision for purposes other than cancer therapy (i.e. tonsillectomy, sleep apnea).
- A routine procedure for tissue collection is planned.
- Ability to understand and the willingness to sign a written informed consent.
Exclusion Criteria:
- Patients without NHL or Hodgkin's disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Collection of tumor tissue to characterize the molecular and cell biology of tumor cells in lymphoma.
Time Frame: The study will continue indefinitely.
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The study will continue indefinitely.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Ronald Levy, MD, Stanford University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
January 1, 1999
Primary Completion (Estimated)
January 1, 2099
Study Completion (Estimated)
January 1, 2099
Study Registration Dates
First Submitted
November 9, 2006
First Submitted That Met QC Criteria
November 9, 2006
First Posted (Estimated)
November 10, 2006
Study Record Updates
Last Update Posted (Actual)
November 22, 2023
Last Update Submitted That Met QC Criteria
November 21, 2023
Last Verified
November 1, 2023
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- LYM0001 (Other Identifier: OnCore)
- 76973 (Other Identifier: Stanford University Alternate IRB Approval Number)
- IRB-13500 (Other Identifier: Stanford IRB)
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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