Erbitux


Website:
http://www.cetuximab.com/
E-mail:

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

School of Nursing, University of Texas at Austin
(512) 471-7971

1700 Red River, Austin, TX, 78701

Website:
http://dscp.nur.utexas.edu/PAIN/
E-mail:eim@mail.nur.utexas.edu

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.

University of Kentucky College of Medicine


Website:
http://www.psyresearchonline.com/crcstudy/index.html
E-mail:

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.

Novartis Pharmaceuticals Corporation
1-888-669-6682


Website:
http://www.pharma.us.novartis.com/
E-mail:

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.

American College of Surgeons Oncology Group
919 668 8400


Website:
http://www.acosog.org
E-mail:

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.

Greenebaum Cancer Center
1-800-492-5538.

UNIVERSITY OF MARYLAND MEDICINE
22 South Greene Street
Baltimore, MD 21201

Website:
http://data.umms.org/scripts/trials
E-mail:

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


Indiana University Hospital
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:

  1. Must be 65-80 years of age
  2. Females must be postmenopausal(no menstrual periods for at least one year; patienst on regular hormone replacement therapy; surgical intervention)


Disqualifying Criteria:
  1. Test for blood in stool within one year.
  2. Rectal Bleeding (hematochezia or melena) within the past one month.
  3. Colonoscopy, colon x-ray, or sigmoidoscopy within the past 10 years.
  4. Surgical Removal of any section of the colon, for any reason.
  5. Coagulopathy (blood clotting disorders) or required use of blood thinners (Prophylactic use of Asprin allowed.
  6. Lung or digestive tract cancer within the past 5 years.
  7. Contraindications to colonoscopy (health conditions that would not allow undergoing a colonoscopy).
  8. High risk conditions for colorectal cancer (familial adenomatous polyposis, hereditary non polposis colorectal cancer syndrome, other heredity cancer syndromes, prior colorectal cancer or adenoma, inflammatory bowel disease, and should have had no more than one first degree relative with colorectal cancer).
  9. Unwilling to have any of the following tests if required (These tests would be paid for completely by the study): Upper Endoscopy, CT of the chest and abdomen, small intestine x-ray.
  10. Chemotherapy within the past 3 months.

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

Colorectal Cancer Study

Study Name
Inheritance of Colon Cancer: A Sibling Pair Study

Description
This multi-center colorectal cancer research study is designed to identify new genes that cause inherited colon cancer. The study will compare genetic material from brothers and sisters (sibling pairs) who have had colon cancer.

 

Eligible candidates must:

 

Participants will:

 

Principal Investigator
Constance Griffin, M.D.

Contact Information
Study Coordinator, Miriam A. Tillery

The Johns Hopkins University

2024 East Monument Street – Suite 2-611

Baltimore, MD 21205-2223

410-614-6334 or toll free 877-880-6188

www.MACGN.org

please contact me if you or anyone you know is interested in our research study!


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