Follow-up Protocol for Patients With Cancer/AIDS/Skin Disease
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT00001503|
Recruitment Status : Enrolling by invitation
First Posted : November 4, 1999
Last Update Posted : December 19, 2018
|Condition or disease|
|Melanoma Ovarian Cancer Prostate Cancer Breast Cancer Lymphoma|
- Patients enrolled on CCR clinical protocols may require long term follow-up to assess outcome (e.g., survival) or the effects of prior therapy.
- Keeping the primary treatment protocols open after accrual is complete in order to follow patients for long term outcome is an administrative burden on investigators and the IRB.
-To provide follow-up for patients who are long term survivors previously enrolled Center for Cancer Research (CCR) trial but who may not currently be enrolled on a research protocol.
-Patients who were previously enrolled on a CCR protocol and who are not eligible for an active NCI intramural primary research protocol.
- The medical procedures/tests will be based on the patient's diagnosis, treatment and supporting clinical information. This is a follow-up study in which only standard tests and procedures are to be performed.
- Clinical information that is relevant to the patients prior protocols will be collected for research purposes.
- Procedures that entail more than minimal risk to the patient should not be performed for research purposes on this protocol.
|Study Type :||Observational|
|Actual Enrollment :||1004 participants|
|Official Title:||Follow-up for Patients Previously Enrolled on the Center for Cancer Research Protocols|
|Actual Study Start Date :||September 19, 1996|
1/ All Patients
Patients who were previously enrolled on a CCR protocol and need follow-up by CCRInvestigators.
- To provide follow-up for patients who are long term survivors previously enrolled Center for Cancer Research (CCR) trial but who may not currently be enrolled on a research protocol [ Time Frame: 30 years ]Provision of a mechanism to follow selected CCR patients when their protocols have been terminated.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00001503
|United States, Maryland|
|National Institutes of Health Clinical Center, 9000 Rockville Pike|
|Bethesda, Maryland, United States, 20892|
|Principal Investigator:||Caryn Steakley, R.N.||National Cancer Institute (NCI)|