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Erbitux
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The program is operational at 27 sites currently and has expanded to include 50 patients/month. Information is available at a special site that was set up by Imclone (http://www.cetuximab.com). Patients can learn how it works (at http://www.Imclone.com) and can get information on how to enter the expanded access program for patients that have exhausted all other treatment avenues at the cetuximab site. Cetuximab trials for those who have not exhausted treatment options are also listed |
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School of Nursing, University of Texas at Austin
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Eun-Ok Im, MPH, PhD, School of Nursing, University of Texas at Austin and her colleagues are conducting a study ultimately aiming at development of computer software to assist nurses' decision making on cancer pain. In the study, Internet survey and online forum discussions using a Web site (home-page) will be conducted to get information on cancer pain of cancer patients from diverse cultural groups. You are being asked to participate in this study because you have been identified as online cancer patients aged at least 18 years who can read and write English and whose self-reported ethnic identity is Hispanic, non-Hispanic (N-H) White, N-H African-American, or N-H Asian. Data will be collected from September 15, 2003 to December 31, 2005. Your involvement will be: (a) about 30 minutes are usually needed to complete the Internet survey questionnaire; and (b) online forums will be conducted for 7 months (6 months for 9 topics and 1 month for additional topics that the participants may add) if you agree to participate in an additional online forum discussion. Your participation is asynchronous (participants can visit the online forum site and read and post messages at their convenience). Methods for the data collection phase include an Internet survey among 400 cancer patients in the U.S. on the Internet and online forum discussions among four ethnically different online forum groups (30 members per group at the beginning). Reimbursement for participation will be made by providing 10 dollars of gift certificate per Internet survey participant and 50 dollars of gift certificate per online forum participant. To get reimbursed for the online forums, at least two messages per topic should be posted. For more information, please visit at our Web-site (http://dscp.nur.utexas.edu/PAIN/) and/or contact us. |
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University of Kentucky College of Medicine
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The study investigates treatment adherence behaviors and quality of life in colorectal cancer patients/survivors. Specifically, we examine the relationship of several variables to treatment adherence and quality of life: (a) marital relationship, (b) emotion regulation and mood, (c) treatment perceptions, and (d) self-efficacy. We intend to have both patients and their spouses/partners complete the on-line survey. This study has been reviewed and given approval by the Office of Research Integrity at the University of Kentucky. The study is completely voluntary and totally anonymous. We do not ask respondents for any identifying information such as name, email address, etc. Individuals who log onto the site may quit at any time by simply closing their browser. |
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Novartis Pharmaceuticals Corporation
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Disease area: Oncology Disease/condition: Colorectal Cancer Patient participation: U Until disease progression or until physician/patient decide treatment is no longer beneficial. Description: This study is being conducted to compare the progression free survival in patients being treated with combination chemotherapy plus an investigational drug versus combination chemotherapy plus placebo. In order to participate in this trial, patients must: • be 18 years of age or older. • Have a confirmed diagnosis of cancer of the colon or rectum with metastatic disease. • be receiving chemotherapy treatment for the first time. Disease area: Oncology Disease/condition: Colorectal Cancer Patient participation: Until disease progression or until physician/patient decide treatment is no longer beneficial. Description: This study is being conducted to determine the overall survival rates of patients with previously treated metastatic adenocarcinoma of the colon or rectum treated with chemotherapy plus an investigational drug versus patients treated with chemotherapy plus placebo. In order to participate in this trial, patients must: • be 18 years of age or older. • have a confirmed diagnosis of cancer of the colon or rectum with metastatic disease. • have been previously treated with chemotherapy. |
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American College of Surgeons Oncology Group
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ACOSOG has activated "A Prospective Study of the Prognostic Significance of Microsatellite Instability in Patients with Early Age-of-Onset Colorectal Cancer". Please refer to the Studies section of the ACOSOG web site at http://www.acosog.org to download the Z0190 protocol, model consent form document, and case report forms. Please refer to the Institutional Review Board Approval SOP for IRB submission and approval guidelines. |
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Greenebaum Cancer Center
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Greenebaum Cancer Center Current Clinical Trials for Colon, Colorectal, Rectal GCC 9818 - A Phase II Study of CPT-11, 5-Fluorouracil, and Leucovorin in Advanced Colorectal Cancer GCC 9842 - Phase I Study of CPT-11, Xeloda, and Radiation Therapy for Colorectal Cancer
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Indiana University Hospital Colorectal Cancer Study Study Name
DISEASE (lay term): Healthy Patient
PURPOSE: To primarily focus in on the detection of Colon cancer and possible cancers of the digestive tract.
INVESTIGATOR: Douglas K. Rex, M.D.
TO QUALIFY YOU MUST:
Eligibility Criteria:
Disqualifying Criteria:
LENGTH/DURATION: Approximately 1 month
LOCATION:
Indiana University Hospital
BENEFITS:
Colonoscopy: Free Colonoscopy; Pathology charges not covered by insurance are the responsibility of the patient.
COMPENSATION:
None
WHO TO CONTACT:
NAME: Beverly Ann Flamme
PHONE: (317) 278-3806
E-MAIL: bflamme@iupui.edu
VERSION DATE: June 27, 2003
Inheritance of Colon Cancer: A Sibling Pair Study
Description
Eligible candidates must:
Participants will:
Principal Investigator
Contact Information
The Johns Hopkins University
2024 East Monument Street – Suite 2-611
Baltimore, MD 21205-2223
410-614-6334 or toll free 877-880-6188
please contact me if you or anyone you know is interested in our research study!